Contour Electrodes, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Contour Electrodes, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Contour Electrodes, Inc. has 4 FDA 510(k) cleared medical devices. Based in Herrin, US.
Historical record: 4 cleared submissions from 1987 to 1990. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Contour Electrodes, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Contour Electrodes, Inc.
4 devices
Cleared
Jul 31, 1990
PHANTOM RADIOTRANSLUCENT ECG MONITORING ELECTRODE
Cardiovascular
168d
Cleared
Jun 20, 1989
L30-LB- INFANT LIMB BAND
Cardiovascular
53d
Cleared
Apr 11, 1988
SOFT-E SERIES T-10 ACCUTRACE TAB RESTING ELECTRODE
Cardiovascular
34d
Cleared
May 12, 1987
CONTOUR SOFT-E SERIES CONDUCTIVE SOLID GEL ELECTRO
Cardiovascular
34d