FDA 510(k) clearances — page 1680
clearances on record, most recent first.
Clearances — page 1680
167,901–168,000 of 175,890- K800211 — IMMUNOGLOBULIN A REAGENT SYSTEM
- K800212 — COMPLEMENT C3 REAGENT SYSTEM
- K800248 — SURGITEK FOERSTER FACE LIFT BANDAGE
- K800249 — SURGITEK FOERSTER MAMMARY BANDAGE
- K800273 — ACUFEX FORCEPS
- K800274 — ACUFEX PROBES
- K800275 — CEBOTOME DRILL
- K800291 — ENDEX REAMERS PULP CANAL, ENDODONTIC
- K800292 — ENDEX BROACH, ENDODONTIC
- K800293 — FILE, PULP CANAL
- K792373 — IPCO M-101 ECHOCARDIOGRAPH (IPCO ULTRA-
- K792460 — CALBIOCHEM-BEHRING RIA-COUNT
- K792606 — WHOLE BLOOD PLATELET CONTROL NORMAL,
- K800075 — MICROMEDIC PUNCH & ELUTER
- K800085 — SYSTEM 203 CHEMISTRY ANALYZER
- K800106 — LUTEINIZING HORMONE RADIOIMMUNOASSAY SYS
- K800107 — FOLLICLE STIMULATING HORMONE
- K800111 — CO2 CONTENT
- K800115 — DURAZYME GPT/ALT
- K800116 — DURAZYME GOT/AST
- K800120 — LDH (L-P) REAGENT
- K800123 — DEXTEX II STERILIZATION WRAP
- K800126 — RSL (125 L) PROGESTERONE KIT
- K800127 — CENTRIFICHEM CK
- K800128 — CENTRIFICHEM BUN
- K800129 — CENTRIFICHEM CREATININE
- K800130 — CENTRIFICHEM URIC ACID
- K800138 — TS-301 THREE-WAY PULP TESTER
- K800141 — ACCUSTROKE PIPET
- K800156 — STAPHYLOCOCCUS MED. 110
- K800157 — BISMUTH SULFITE AGAR
- K800158 — AZIDE BLOOD AGAR BASE W/&WTHOT SHP. BLD
- K800165 — VENTRE/SEP T3 UPTAKE RADIOASSAY
- K800169 — AMES RIALYZE - CHROMATOGRAPHY TUBES
- K800170 — AMES RIALYZE - UPTAKE CHROM. TUBES
- K800174 — GAMBRO LUNDIA COIL DIALYZER
- K800187 — EMC-M-175, THYROXINE - 100 TUBES
- K800188 — EMC-M-180, T3 UPTAKE - 100 TUBES
- K800189 — BOVINE ALBUMIN 22% & 30% SOLUTIONS
- K800190 — STANBIO DIRECT URIC ACID TEST SET #0770
- K800215 — CULTURIA MACCONKEY/CLED #DM87
- K800240 — SEROCLUSTER U AND V
- K792646 — AMP DIRECT VASCULAR MONITORING SYSTEM
- K792669 — COROMETRICS-PUSH BUTTON SPIRAL ELECTRODE
- K800022 — MODEL 807 SUCTION CAUTERY FINGER TIP
- K800057 — MICRO ELISA MINI READER
- K800062 — PIPET CALIBRATION KIT
- K800091 — COMBISON 100-MODEL 100 & 110
- K800093 — TRANSDUCER
- K800094 — COMBISON 200 & COMBISON 202
- K800095 — MGD-3
- K800096 — AMBIVASON DR-200
- K800097 — MINIVASON 9
- K800098 — MINIFETON 200
- K800105 — TELESONIC (HEARING AID)
- K800113 — SEARS BEHIND-THE-EAR HEARING AID
- K800117 — TRU-PULSE PADS
- K800131 — CENTRIFICHEM ALP/ALKALINE PHOSPHATASE
- K800139 — SEARLE PHO/SONIC ALPHA 2000
- K800162 — ONCE TM
- K800177 — I.M. BLADES
- K800179 — INFRASONDE AUTO/INFLATOR ELEC. VIBRATOR
- K800184 — OXFORD EXTERNAL FIXATION SYSTEM
- K800194 — OVALITH P-BP BIPOLAR CARDIAC PACEMAKER
- K800195 — COTTON UNDER CAST PADDING
- K800207 — UHR UNIVERSAL6HIP REPLACEMENT
- K792270 — DEXIDE DISPOSABLE PREP STICK W/IODOPHOR
- K792520 — ANESTHESIA & HOSPITAL SYRINGE HOLDER
- K791512 — CONTINUOUS AMBULATORY DIALYSIS (CAPD)
- K792597 — RECTAL LEAKAGE INHIBITOR
- K792611 — GAMBRO LUNDIA PLATE DIALYZER
- K792648 — UNILAB CULTURING SET
- K792651 — CAPD TRANSFER SET JC9044
- K800104 — ROYCO MODEL 951 CELL MIXER
- K800110 — X-FLO
- K800153 — EXTEMP/EXTEMP-V
- K800210 — TONGUE HOLDER/SALIVA EJECTOR
- K792269 — WRIGHT DOW CORNING SOFTGOODS W/DOW
- K792418 — SHARPLAN 743, CO2 LASER SURGICAL SYSTEM
- K792451 — PNEUPAC RESUSCITATOR INSTANT ACTION SET
- K792452 — PNEUPAC RESUSCITATOR INSTANT ACTION SET
- K792453 — PNEUPAC OXYGEN THERAPY UNIT
- K792454 — PNEUPAC RESUSCITATOR INSTANT ACTION SET
- K792455 — PNEUPAC VENTILATOR/RESUSCITATOR #2
- K792456 — PNEUPAC VENTILATOR/RESUSCITATOR #3
- K792457 — COMPRESSOR
- K792458 — PNEUPAC TEST SET, PT.#500-A250
- K792459 — PNEUPAC VENTILATOR/RESUSCITATOR
- K792488 — ECA GEL
- K792489 — UCA CREAM
- K792491 — ECA CREAM
- K792492 — UCA GEL
- K792526 — PULSE GENERATOR, MODEL NO. LIT 222
- K792565 — SORIN PULSE GENERATOR MODEL # LIT 214 H
- K792619 — RMC KNEE METAL SHOE TIBIAL COMPONENTS
- K800031 — PERMADYNE POLYETHER RUBBER IMPRESSION
- K800037 — PLATELET RETENTION (ADHESION) COLUMNS
- K800054 — KODAK EKTACHEM ELECTROLYTE ANALYZER
- K800065 — ASI REAGENT
- K800068 — ELECTRICAL MUSCLE STIMULATOR (EMS)
Data sourced from openFDA. This site is unofficial and independent of the FDA.