Medi-Tech, Inc. - FDA 510(k) Cleared Devices
36
Total
35
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medi-Tech, Inc. General & Plastic Surgery ✕
4 devices
Cleared
Nov 02, 1989
MODIFIED LABELING TO THE SPAND-GEL GRANULATED GEL
General & Plastic Surgery
34d
Cleared
Jun 10, 1982
HYPODERMIC NEEDLES & SYRINGES
General & Plastic Surgery
36d
Cleared
Jun 02, 1981
PERCUTANEOUS DRAINING CATHETER
General & Plastic Surgery
18d
Cleared
Mar 06, 1979
CATHETER, TRANSLUMINAL BALLOON
General & Plastic Surgery
141d