Medi-Tech, Inc.
Medi-Tech, Inc. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1996.
Top product codes for Medi-Tech, Inc.
Recent clearances by Medi-Tech, Inc.
- K954457 — MEDI-TECH EDDY INTRAVASCULAR INFUSION CATHETER
- K952345 — MEDI-TECH PLATFORM GUIDE CATHETER
- K952056 — IMMUNOASSAY DRUGS OF ABUSE CONTROLS
- K945289 — DOA - IMMUNOASSAY CUT-OFF CALIBRATOR
- K942551 — THERAPEUTIC DRUG MONITORING CONTROL, ASSAYED
- K943290 — BILIRUBIN PLUS/PEDIATRIC CONTROLS
- K922990 — HEMODIALYSIS BATH
- K942552 — THERAPEUTIC DRUG MONITORING CONTROL, UNASSAYED
- K904073 — COAGULATION REFERENCE PLASMA, ABNORMAL
- K895819 — MODIFIED LABELING TO THE SPAND-GEL GRANULATED GEL
- K873295 — PROSTATIC URETHRO. BALLOON DILATATION CATHETER
- K884354 — IMAGER FLUSH CATHETERS
- K883880 — KATZEN THROMBOLYSIS GUIDEWIRE
- K884513 — PF TEST
- K874096 — TITANIUM GREENFIELD VENA CAVA FILTER CARRIER
- K883118 — ON THE SPOT CANDIDASURE
- K880298 — PERIPHERAL DILATATION CATHETER
- K864118 — MEDI-TECH SELECTIVE TORQUE CATHETER
- K870729 — TITANIUM PERCUTANEOUS GREENFIELD VENA CAVE FILTER
- K861599 — T-FASTENER
- K852097 — PERCUTANEOUS GREENFIELD VENA CAVA FILTER SYSTEM
- K852552 — COONS GASTROSTICK SYSTEM
- K851402 — LEVEEN INFLATOR DISPOSABLE INFLATION SYRINGE
- K843012 — WIREGUIDE OR GUIDEWIRE
- K844292 — MEDI-TECH DILATATION CATHETERS
- K843383 — MEDI-TECH DILATATION CATHETERS
- K842890 — PERCUFIX CATHETER CUFF
- K842205 — OXY-VAC
- K830483 — COONS SOFT STENT
- K821816 — ANGIOGRAPHIC CATHETER
- K821348 — HYPODERMIC NEEDLES & SYRINGES
- K812279 — ENTER-A1 ENTERIC FEEDING TUBE
- K811378 — PERCUTANEOUS DRAINING CATHETER
- K810336 — POLYPECTOMY SNARE
- K781772 — CATHETER, TRANSLUMINAL BALLOON
- K781780 — CATHETER, EXTERNAL MALE NURSING CARE
Data sourced from openFDA. This site is unofficial and independent of the FDA.