Hancock Laboratories, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Hancock Laboratories, Inc. Cardiovascular ✕
5 devices
Cleared
Sep 09, 1980
HANCOCK * OBTURATORS
Cardiovascular
33d
Cleared
Apr 08, 1980
MODIFIED CATHETER PACKAGE
Cardiovascular
12d
Cleared
Feb 01, 1980
HANCOCK AORTIC PUNCH
Cardiovascular
14d
Cleared
Mar 26, 1979
MERSILENE SUTURES
Cardiovascular
13d
Cleared
May 26, 1978
DURAN FLEXIBLE RING
Cardiovascular
46d