K-Med, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
K-Med, Inc. has 4 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 4 cleared submissions from 1981 to 1983. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by K-Med, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - K-Med, Inc.
4 devices
Cleared
Nov 28, 1983
COAXIAL ELECTRODE #300A
Gastroenterology & Urology
118d
Cleared
Aug 31, 1981
K-MED SILICONE SUMP DRAIN W/ SHEATH
General & Plastic Surgery
42d
Cleared
Aug 31, 1981
K-MED SILICONE SUMP DRAIN
General & Plastic Surgery
42d
Cleared
May 13, 1981
K-MED ENCOURAGER INCENTIVE SPIROMETER
Anesthesiology
64d