C.R. Bard, Inc.
FDA 510(k) medical device clearances.
Clearances by C.R. Bard, Inc. — page 7
601–646 of 646- K781766 — UTERINE SOUND, BURNETT DISPOSABLE
- K781767 — INSTRUMENT CURNETT MINI-CONER BIOPSY
- K781954 — CATHETER INTRODUCERS, ARTERISE
- K781838 — CALCULATOR, WITH CHARGER
- K781736 — DISC, COLOPLAST PRE-OP STOMA
- K781577 — DISPOSABLE CARDIOTOMY; H-700F, H-700
- K780438 — SAFETY SPRING GUIDES, TEFLON COATED
- K780630 — CONTROLLER, SERVO, INSPIRON
- K780409 — COLOPLAST-DURASEAL OSTOMY APPLIANCE
- K780057 — URINE SAMPLE COLLECTION KIT
- K780167 — CATH KIT, URINE SPECIMEN
- K780056 — OXYGENATOR HOLDER
- K772338 — SYRINGE, BLOOD, SAMPLING, ARTERIAL
- K772294 — INSPIRON MANIFOLD (DOUBLE)
- K772295 — INSPIRON MANIFOLD (SINGLE)
- K772296 — INSPIRON MANIFOLD
- K780032 — URINARY LEG BAG
- K772150 — DIALYSIS DRAINAGE UNIT, PERITONEAL
- K771393 — ELHCTRONIC SPHYGMOMANOMETER
- K771394 — ELECTRONIC STETHESCOPE
- K771776 — ECG CLUSTER ELECTRODE
- K771352 — ELECTROSURG. PATIENT GROUNDING PLATE
- K770814 — CATHETER, URETHERAL
- K770943 — ENDOSCOPE, UROLOGICAL, FEMALE
- K771825 — CARBA LINGUARDUC
- K771750 — RF CHOKE CABLE
- K771775 — COLORPLAST TRANSVERSE SYSTEM
- K771261 — ADVANSET
- K771440 — MACBICK CONDUCTIVE GEL - 000907
- K771074 — NASAL OXYGEN CANNULA, #017207
- K771075 — OXYGEN CONNECTING TUBE #017205
- K771149 — ENDOMETRIAL ASPIRATION BIOSPY KIT 182341
- K770647 — ELECTROSURGICAL GROUNDING CABLE
- K770646 — ELECTROSURGICAL PATIENT GROUNDING PAD
- K770514 — STERILIZER WRAP
- K760997 — UNDER BOTTOCKS DRAPE
- K761083 — BARD URINE METER W/ BAG
- K760662 — STERIL.WRAP(#221901,2,3,4,5,6,7,8,9)
- K760661 — STERILIZER WRAP (CAT#221831,2,3,4,5,6)
- K760736 — BARIMEX, BARIUM SULFATE COMPOUND
- K760455 — OBSTETRICAL PACK (VIGILON OB PACK)
- K760093 — CATHETER, SILICONE FOLEY (BARDEX)
- K760216 — SUCTION INSTRUMENT, MACBICK POOLE TIP
- K760217 — SUCTION INSTRUMENT, MACBICK DIS. FRAZ.
- K760253 — TRAY, UNIVERSAL FOLY WO/DRAINAGE BAG
- K760254 — TRAY, FOLEY CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.