Conmed Andover Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Conmed Andover Medical, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Conmed Andover Medical, Inc. has 8 FDA 510(k) cleared medical devices. Based in Haverhill, US.
Historical record: 8 cleared submissions from 1994 to 1995. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Conmed Andover Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Conmed Andover Medical, Inc.
8 devices
Cleared
Jun 20, 1995
1800 MONITORING ECG ELECTRODE AND 1870 DIAPHORETIC MONITORING ECG ELECTRODES
Cardiovascular
203d
Cleared
May 17, 1995
1700 MONITORING ECG ELECTRODE
Cardiovascular
146d
Cleared
Nov 22, 1994
ECG ELECTRODE
Cardiovascular
62d
Cleared
Nov 22, 1994
1710 MONITORING ECG ELECTRODE
Cardiovascular
57d
Cleared
Oct 17, 1994
2700 CLEARTRACE RADIOTRANSLUCENT MONITORING ECG ELECTROBE
Cardiovascular
17d
Cleared
Sep 22, 1994
CLOTH TENS/BNES ELECTRODE
Neurology
105d
Cleared
Jul 27, 1994
DISPOSABLE SURGICAL CABLE
Cardiovascular
105d
Cleared
Jul 20, 1994
CONMED ANDOVER MED ECG ELECTRODES
Cardiovascular
28d