Copal, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Copal, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Copal, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1982 to 1984. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Copal, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Copal, Inc.
5 devices
Cleared
Apr 19, 1984
DIGITAL SPHYGMOMANOMETER UA-231
Cardiovascular
251d
Cleared
Apr 17, 1984
DIGITAL SPHYGMOMANOMETER UA-251
Cardiovascular
249d
Cleared
Apr 17, 1984
DIGITAL SPHGMOMANOMETER UA-271
Cardiovascular
249d
Cleared
Dec 22, 1983
ACTIMETER UB-103
Cardiovascular
132d
Cleared
Mar 25, 1982
ELECTRONIC DIGITAL SPHYGMOMANOMETER
Cardiovascular
49d