Medi-Tech, Inc.

FDA 510(k) & PMA Approved Devices — 36 products

Total Devices36

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K954457	MEDI-TECH EDDY INTRAVASCULAR INFUSION CATHETER	KRA	1996-05-15	View
510(k)	K952345	MEDI-TECH PLATFORM GUIDE CATHETER	DQY	1995-08-17	View
510(k)	K952056	IMMUNOASSAY DRUGS OF ABUSE CONTROLS	DIF	1995-06-01	View
510(k)	K945289	DOA - IMMUNOASSAY CUT-OFF CALIBRATOR	DKB	1994-12-13	View
510(k)	K942551	THERAPEUTIC DRUG MONITORING CONTROL, ASSAYED	DIF	1994-10-06	View
510(k)	K943290	BILIRUBIN PLUS/PEDIATRIC CONTROLS	JJY	1994-09-14	View
510(k)	K922990	HEMODIALYSIS BATH	KPO	1994-09-12	View
510(k)	K942552	THERAPEUTIC DRUG MONITORING CONTROL, UNASSAYED	DIF	1994-09-09	View
510(k)	K904073	COAGULATION REFERENCE PLASMA, ABNORMAL	GGC	1990-10-22	View
510(k)	K895819	MODIFIED LABELING TO THE SPAND-GEL GRANULATED GEL	KMF	1989-11-02	View
510(k)	K873295	PROSTATIC URETHRO. BALLOON DILATATION CATHETER	KOE	1989-07-31	View
510(k)	K884354	IMAGER FLUSH CATHETERS	DQO	1989-04-21	View
510(k)	K883880	KATZEN THROMBOLYSIS GUIDEWIRE	DQX	1989-04-06	View
510(k)	K884513	PF TEST	GMZ	1989-02-03	View
510(k)	K874096	TITANIUM GREENFIELD VENA CAVA FILTER CARRIER	DTK	1988-11-04	View
510(k)	K883118	ON THE SPOT CANDIDASURE	LRF	1988-09-30	View
510(k)	K880298	PERIPHERAL DILATATION CATHETER	LIT	1988-04-22	View
510(k)	K870729	TITANIUM PERCUTANEOUS GREENFIELD VENA CAVE FILTER	DTK	1987-04-09	View
510(k)	K864118	MEDI-TECH SELECTIVE TORQUE CATHETER	DQY	1987-04-09	View
510(k)	K861599	T-FASTENER	KNT	1986-10-02	View