Medi-Tech, Inc. - FDA 510(k) Cleared Devices
36
Total
35
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medi-Tech, Inc. Gastroenterology & Urology ✕
9 devices
Cleared
Sep 12, 1994
HEMODIALYSIS BATH
Gastroenterology & Urology
812d
Cleared
Jul 31, 1989
PROSTATIC URETHRO. BALLOON DILATATION CATHETER
Gastroenterology & Urology
714d
Cleared
Oct 02, 1986
T-FASTENER
Gastroenterology & Urology
156d
Cleared
Oct 17, 1985
COONS GASTROSTICK SYSTEM
Gastroenterology & Urology
122d
Cleared
Sep 04, 1984
PERCUFIX CATHETER CUFF
Gastroenterology & Urology
43d
Cleared
Mar 09, 1983
COONS SOFT STENT
Gastroenterology & Urology
22d
Cleared
Aug 25, 1981
ENTER-A1 ENTERIC FEEDING TUBE
Gastroenterology & Urology
12d
Cleared
Mar 20, 1981
POLYPECTOMY SNARE
Gastroenterology & Urology
39d
Cleared
Dec 07, 1978
CATHETER, EXTERNAL MALE NURSING CARE
Gastroenterology & Urology
50d