Medtech Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medtech Intl., Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Medtech Intl., Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1978 to 1992. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medtech Intl., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medtech Intl., Inc.
6 devices
Cleared
Dec 11, 1992
CUT RESISTANT GLOVES OR SURGICAL GLOVE LINER
General Hospital
289d
Cleared
Jan 09, 1986
IV MATE
General Hospital
115d
Cleared
Sep 24, 1979
HYPERDERMIC NEEDLE WITH SENSOR #514
General Hospital
70d
Cleared
Mar 26, 1979
GAUZE & COTTON SPONGES
General & Plastic Surgery
28d
Cleared
Mar 26, 1979
SURGICAL EYE SPONGE
General & Plastic Surgery
21d
Cleared
Sep 20, 1978
STIMULATOR, NERVE, TRANSCUTANEOUS
Neurology
77d