North Coast Medi-Tek is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
North Coast Medi-Tek - FDA 510(k) Cleared Devices
6
Total
4
Cleared
0
Denied
North Coast Medi-Tek has 4 FDA 510(k) cleared medical devices. Based in Eastlake, US.
Historical record: 4 cleared submissions from 1985 to 1987. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by North Coast Medi-Tek Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - North Coast Medi-Tek
6 devices
Cleared
May 11, 1987
IVR-SP CUSTOM ANGIOGRAPHY TRAY
Cardiovascular
97d
Cleared
Apr 14, 1987
PTC-6 AND PTC-8 PERCUTANEOUS CHOLANGIOGRAPHY
General & Plastic Surgery
70d
Cleared
Apr 06, 1987
LP EXTENSION SETS
General Hospital
62d
Cleared
Mar 17, 1987
MYA-1 AND MYT-1 MYELOGRAM TRAY
Cardiovascular
42d
Cleared
Mar 05, 1987
RCT-1, RCT-2, RCT-3 ARTHROGRAM TRAY
General & Plastic Surgery
30d
Cleared
Nov 25, 1985
BIOPSY TRAY I & II
General & Plastic Surgery
49d