Johnson & Johnson Professionals, Inc.
Johnson & Johnson Professionals, Inc. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 2000.
Top product codes for Johnson & Johnson Professionals, Inc.
Recent clearances by Johnson & Johnson Professionals, Inc.
1–100 of 206- K992173 — SIPHONGUARD CSF CONTROL DEVICE
- K991413 — CODMAN ETHISORB DURA PATCH
- K991222 — CODMAN MICROSENSOR VENTRICULAR CATHETER KIT
- K982379 — SUNDT SLIM-LINE ANEURYSM CLIP APPLIER
- K982812 — G2 TOTAL HIP SYSTEM FEMORAL STEM (11/13 TAPER)
- K983141 — CAPITELLO-CONDYLAR TOTAL ELBOW PROSTHESIS
- K983014 — SUMMIT ACETABULAR SYSTEM
- K980778 — HAKIM MICRO PROGRAMMABLE VALVE SYSTEM
- K974739 — HAKIM PROGRAMMABLE VALVE SYSTEM
- K980801 — J-FX BIPOLAR HEAD
- K980081 — S-ROM ZIRCONIA CERAMIC FEMORAL HIP HEAD
- K980286 — ULTIMA ACETABULAR ROOF REINFORCEMENT RING
- K974331 — UNI-ROM TOTAL HIP SYSTEM FEMORAL STEM
- K974088 — CODMAN INTRACRANIAL BOLT
- K973774 — CODMAN HAKIM MICRO PRECISION VALVE
- K973307 — S-ROM ZIRCONIA CERAMIC FEMORAL HIP HEAD
- K972435 — ULTIMA AND ULTIMA LX CEMENTED FEMORAL STEM
- K971189 — P.F.C. SIGMA KNEE SYSTEM (SIZE 1.5)
- K971652 — P.F.C. SIGMA INSET PATELLA
- K971682 — J-FX CERCLAGE SYSTEM
- K964923 — CODMAN LUMBAR DRAINAGE CATHETER KIT
- K964795 — CEMENTED CALCAR REPLACEMENT FEMORAL STEM
- K965156 — ULTIMA*UNIPOLAR HEAD AND ADAPTER SLEEVES
- K963885 — ULTIMA FX FEMORAL HIP STEMS
- K963117 — P.F.C. CRUCIATE RETAING KNEE SYSTEM
- K963206 — S-ROM HIP SYSTEM - LOCKING PLUG
- K954481 — P.F.C. UNI-COMPARTMENTAL KNEE SYSTEM
- K963499 — MIRROR FINISH BIPOLAR FORCEPS
- K962429 — SAFETY VEST
- K962248 — P.F.C. CERAMIC HIP HEAD
- K961939 — S-ROM FEMORAL HIP STEM(SIZES 12 X 06 X 115 AND 12 X 07 X 115)
- K961685 — P.F.C. CRUCIATE RETAINING KNEE SYSTEM (SIZE 1.5)
- K945518 — P.F.C. 2 TOTAL HIP SYSTEM POROUS COATED MODULAR FEMORAL COMPONENT
- K952859 — ULTIMA CEMENTED LONG STEM FEMORAL COMPONENT
- K953200 — ULTIMA SIZE 0 CEMENTED FEMORAL STEM
- K953202 — P.F.C. SIZE 0 CEMENTED FEMORAL COMPONENT
- K955385 — JOHNSON & JOHNSON AUSTIN MOORE STEM
- K944544 — ABSORBABLE BONE SCREW
- K952830 — DARWIN KNEE SYSTEM (TC3)
- K954699 — BRAY RONGEUR
- K954851 — BIOPOLAR FORCEPS LINE
- K953730 — CODMAN ANTERIOR CERVICAL PLATE SYSTEM
- K945585 — COMAN(R) CU-11 MODEL NUMBER 82-6634
- K954021 — EXTERNAL DRAINAGE SYSTEM (EDS AND EDS II)
- K944222 — CODMAN-MEDOS VALVE SHUNT SYSTEM
- K952161 — BIPOLAR COAGULATION INSTRUMENT
- K950563 — ULTIMA AUGMENTED UHMWPE CUP
- K951934 — PFC CEMENT RESTRICTOR
- K950010 — DARWIN KNEE SYSTEM (CRUCIATE SUBSTITUTING) POROUS COATED AND NON-POROUS COATED
- K945793 — P.F.C.(R) BIPOLAR HIP SYSTEM - 22MM BIPOLAR
- K945572 — CODMAN(R) RIDIG AND STEERABLE ENDOSCOPE HOLDER, MODEL 83-1352
- K944132 — P.F.C. TOTAL HIP SYSTEM
- K943462 — DARWIN KNEE SYSTEM
- K943906 — P.F.C. CEMENT PRESSURIZING SYSTEM
- K944769 — P.F.C. APICAL PLUG
- K942060 — P.F.C. CEMENT RESTRICTOR
- K934860 — TI-FRAME
- K894937 — SHAW KNEE MODULAR TIBIAL TRAY-POROUS
- K895861 — DELTA-TECH(TM) CAST REMOVAL SYSTEM
- K893872 — P.F.C. HIP SYSTEM POROUS COATED FEMORAL COMPONENT
- K892394 — P.F.C. MODULAR KNEE SYSTEM, TIBIAL TRAY-POROUS
- K893562 — A.QC HCT LEVEL 1 AND 2
- K892238 — CLA 200 CHEMPRO(R) LIPID ANALYZER
- K884796 — P.F.C.(TM) MODULAR KNEE SYSTEM
- K882234 — JOHNSON & JOHNSON MODULAR TOTAL KNEE PROSTHESIS
- K881222 — JOHNSON & JOHNSON FLUFF SPONGE
- K880826 — MICROLOC(TM) POROUS COATED UNICONDYLAR KNEE SYSTEM
- K873423 — MAXIMA* COLLAPSIBLE VENOUS RESERVOIR BAG & HOLDER
- K873585 — POROUS COATED ACETABULAR CUP
- K873514 — JOHNSON & JOHNSON BIPOLAR ENDOPROTHESIS
- K872982 — JOHNSON & JOHNSON ABSORBENT OCCLUSIVE DRESSING
- K864912 — PDS (POLYDIOXANON) ABSORBABLE PIN
- K871295 — ADAPTALITE* PORCELAIN VENEER CEMENTATION SYSTEM
- K864226 — JOHNSON & JOHNSON STAINING REMOVING COMPOUND
- K870445 — THREADED ACETABULAR COMPONENT
- K870211 — BONDEX* GLASS IONOMER CEMENT
- K864895 — INTERSEPT* CARDIOTOMY RESERVOIR WITH FILTER
- K862211 — ULTRASOUND TRANSDUCER ASSEMBLY
- K864262 — ARTERIAL 20/40 MICRON FILTERS W/WO HEPARIN COATING
- K864508 — HOWSE II TOTAL HIP REPLACEMENT SYSTEM
- K864008 — ACCLAIM* BRACKET ADHESIVE
- K860009 — 5.0 MHZ MERIDIAN ULTRASOUND IMAGING SYSTEM
- K861358 — PS SYSTEM WITH SD-200 DOPPLER
- K860697 — ULTRASOUND IMAGING SYSTEM MODEL 280 SL
- K861737 — MERIDIAN IMAGING SYSTEM
- K862326 — POROUS COATED HIP FEMORAL PROSTHESIS
- K861710 — MODEL UST-SSD 880L1-5 TRANESOPHAGEAL PHASED ARRAY
- K861833 — RESTOR (COMET)*DENTAL RESTORATIVE
- K862163 — JOHNSON & JOHNSON PETROLATUM GAUZE NON ADHER DRESS
- K861384 — NON-ADHERING DRESSING WITH POVIDONE-IODINE
- K854996 — ULTRASONIC COUPLANT GEL
- K860486 — ACTISORB ACTIVATED CHARCOAL DRESSING
- K860313 — 3.0 MHZ LINEAR ARRAY PROBE MODEL UST 5031
- K854743 — 2.5 MHZ PHASED ARRAY SECTOR MERIDIAN PROBE
- K853240 — MERIDIAN ULTRASOUND IMAGING SYSTEM
- K853702 — ULTRASOUND COUPLANT SHEET/SOLID ULTRASOUND COUPLAN
- K854554 — DELTA-LITE CASTING RESIN
- K854050 — EXCEL BRACKET ADHESIVE
- K854341 — DELTA-LITE CASTING RESIN
- K852362 — UROLOGICAL ULTRASOUND DIAGNOSTIC SYS/EQUIP. SSD-52
Data sourced from openFDA. This site is unofficial and independent of the FDA.