Medi-Tech, Inc. - FDA 510(k) Cleared Devices
36
Total
35
Cleared
0
Denied
Medi-Tech, Inc. has 35 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 35 cleared submissions from 1978 to 1996.
Browse the FDA 510(k) cleared devices submitted by Medi-Tech, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medi-Tech, Inc.
36 devices
Cleared
May 15, 1996
MEDI-TECH EDDY INTRAVASCULAR INFUSION CATHETER
Cardiovascular
233d
Cleared
Aug 17, 1995
MEDI-TECH PLATFORM GUIDE CATHETER
Cardiovascular
90d
Cleared
Jun 01, 1995
IMMUNOASSAY DRUGS OF ABUSE CONTROLS
Toxicology
30d
Cleared
Dec 13, 1994
DOA - IMMUNOASSAY CUT-OFF CALIBRATOR
Toxicology
43d
Cleared
Oct 06, 1994
THERAPEUTIC DRUG MONITORING CONTROL, ASSAYED
Toxicology
128d
Cleared
Sep 14, 1994
BILIRUBIN PLUS/PEDIATRIC CONTROLS
Chemistry
68d
Cleared
Sep 12, 1994
HEMODIALYSIS BATH
Gastroenterology & Urology
812d
Cleared
Sep 09, 1994
THERAPEUTIC DRUG MONITORING CONTROL, UNASSAYED
Toxicology
101d
Cleared
Oct 22, 1990
COAGULATION REFERENCE PLASMA, ABNORMAL
Hematology
47d
Cleared
Nov 02, 1989
MODIFIED LABELING TO THE SPAND-GEL GRANULATED GEL
General & Plastic Surgery
34d
Cleared
Jul 31, 1989
PROSTATIC URETHRO. BALLOON DILATATION CATHETER
Gastroenterology & Urology
714d
Cleared
Apr 21, 1989
IMAGER FLUSH CATHETERS
Cardiovascular
186d