Product code KRA— Cardiovascular
Bullfrog Micro-Infusion Device
- Classification name
- Catheter, Continuous Flush
- Device class
- Class 2
- Regulation
- 21 CFR 870.1210
- Advisory panel
- Cardiovascular
- Total cleared
- 176
- First cleared
- Most recent
Clearances under product code KRA — page 2
101–176 of 176- K024118 — ULTRAFLOW HPC FLOW DIRECTED MICRO CATHETER, MODELS 105-5065 AND 105-5066
- K021591 — PROWLER SELECT (10, 14, AND PLUS) INFUSION CATHETERS WITH AND WITHOUT PRE-SHAPED TIPS
- K020680 — PROWLER SELECT 10 AND 14 INFUSION CATHETERS WITH AND WITHOUT PRE-SHAPED TIPS
- K020733 — PVS 1500 SDS
- K011646 — NEUROEDGE INFUSION CATHETER
- K010004 — FLOWRIDER FLOW DIRECTED MICRO CATHETER, MODEL 105-5065
- K003925 — PROWLER INFUSION CATHETERS WITH PRE-SHAPED TIPS
- K002723 — REBAR MICRO CATHETER: REBAR-10 (1.7F), 153 CM, DUAL MARKER BANDS; REBAR MICRO CATHETER: REBAR-10 (1.7F), 170 CM, DUAL MA
- K994155 — EXCELSIOR 1018 MICROCATHETER
- K001966 — REBAR MICRO CATHETER: REBAR-18 [2.3F], 110 CM, 130 CM, 153 CM, SINGLE MARKER BAND AND 153 CM, DUAL MARKER BAND
- K000177 — RENEGADE HI-FLO MICROCATHETER
- K993672 — REBAR MICRO CATHETER, MODELS 105-5080, 105-5086
- K993266 — PROWLER PLUS INFUSION CATHETER
- K983003 — 1 MASS TRANSIT INFUSION CATHETER, 1 VARIOUS
- K974473 — EASY RIDER MICRO CATHETER
- K980104 — FLOW RIDER FLOW DIRECTED MICRO CATHETER
- K971619 — MICROFUSE MEMBRANE INFUSION CATHETER
- K974222 — CES MASSTRANSIT INFUSION CATHETER
- K973645 — RENEGADE FIBER BRAIDED MICROCATHETER
- K972518 — TRANSIT/RAPIDTRANSIT/SPEEDSTER/PROWLER INFUSION CATHETER
- K971306 — FG INFUSION CATHETER
- K964868 — 2.9F CRAGG-MCNAMARA VALVED INFUSION CATHETER
- K962129 — CONTINUOUS FLUSH DEVICE
- K965189 — SPINNAKER
- K965181 — CES INFUSION CATHETER
- K964154 — SEGUE INFUSION CATHETER
- K963988 — INTRAVASCULAR INFUSION DEVICE
- K961668 — MICROFERRET CATHETER
- K955525 — FLOWER INFUSION CATHETER MODEL F-25/50, F-60/70
- K955534 — SEQUE INFUSION CATHETER (S-25,30,35,40,45,50,60)
- K961294 — SCIMED DISPATCH GOLD CORONARY CATHETER
- K961527 — MX703 AND MX730 CONTINUOUS FLUSH DEVICES
- K954457 — MEDI-TECH EDDY INTRAVASCULAR INFUSION CATHETER
- K953133 — SCIMED DISPATCH CORONARY INFUSION CATHETER
- K954020 — MICRO THERAPEUTICS SIDEHOLE INFUSION WIRE
- K954949 — TRANSIT INFUSION CATHETER WITH SIDEHOLES
- K952874 — TRANSIT INFUSION CATHETER
- K952872 — SSCIMED CORONARY GUIDE WIRE/INFUSION CATHETER
- K945666 — EVOLUTION(TM) MICROCATHETER
- K951602 — PULSE*SPRAY INFUSION SYSTEM
- K945909 — NAVARRE N-FUSER(TM) PERIPHERAL INFUSION CATHETER
- K945904 — SCIMED(R) VENTURE(TM) II INFUSION CATHETER
- K951502 — CVD BULLET INFUSION CATYHETER
- K951503 — CVD BULLETT HI-FLO INFUSION CATHETER
- K945593 — SCIMED(R) CORONARY GUIDE WIRE EXCHANGE/INFUSION CATHETER
- K935349 — LOCALMED INFUSION CATHETER
- K931335 — SCIMED(R) VENTURE(TM) INFUSION CATHETER
- K932800 — CARDIMA TRACKER(R) INFUSION CATHETER
- K932616 — SCIMED(R) DISPATCH(TM) CORONARY INFUSION CATHETER
- K932188 — SAFESET RESERVOIR
- K921247 — ZEPHYR INFUSION CATHETER
- K914751 — SELECTIVE INFUSION II CATHETER
- K924661 — SWAN-GANZ INTELLICATH CCO THERMODILUTION CATHETER
- K923368 — MAGIC INFUSION CATHETER
- K914979 — EDM(R) INFUSION CATHETER
- K905447 — E-Z-EM PULSED INFUSION SYSTEM
- K896819 — VAMP VENOUS/ARTERIAL BLOOD MANAGEMENT PROTECTION
- K885281 — VAMP VENOUS/ARTERIAL BLOOD MANAGEMENT PROTECTION
- K884946 — JEHLE CORONARY PERFUSION CATHETERS
- K874242 — JEHLE CORONARY PERFUSION CATHETERS
- K860570 — ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE
- K832058 — ANGIO-FLO CONTIN-ARTERIAL FLUSH DEV.
- K831730 — CONTINUOUS FLUSH DEVICE
- K831637 — ACCU-FLUSH
- K812173 — FLUSHFLO II
- K811410 — MEDI-TRACE
- K801829 — MEDI-TRACE DISP. FLUSHING DEV./MONITOR
- K801173 — ANGIO-FLO MONITORING KIT
- K791890 — CONTINUOUS FLUSH DEVICE, CAT. #14-370
- K792141 — CONTINUOUS FLUSH DEVICE
- K791844 — CRITIFLO & CRITIFLO DOME
- K790455 — MICROFLUSH
- K790327 — ANGIO-FLO
- K780479 — DELTA-FLOW
- K770432 — MICROFLUSH
- K761273 — FLUSHFLO-MODEL CC1-6
Data sourced from openFDA. This site is unofficial and independent of the FDA.