Kerma Medical Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kerma Medical Products, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Kerma Medical Products, Inc. has 5 FDA 510(k) cleared medical devices. Based in Chesapeake, US.
Historical record: 5 cleared submissions from 1991 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Kerma Medical Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kerma Medical Products, Inc.
5 devices
Cleared
Apr 13, 1994
MOORE SECURE CAP
General Hospital
408d
Cleared
May 29, 1992
MULTIPLE STERILE GAUZE BANDAGE ROLLS, VARI SIZES
General & Plastic Surgery
151d
Cleared
Mar 26, 1992
MULTIPLE DRESSING, STERILE NONADDHERENT PADS
General & Plastic Surgery
87d
Cleared
Dec 04, 1991
MULTIPLE BURN DRESSING
General & Plastic Surgery
84d
Cleared
Dec 04, 1991
STERILE BANDAGE, GAUZE, FINE MESH, 3X8 INCHES
General & Plastic Surgery
30d