Contour Medical Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Contour Medical Technology, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Contour Medical Technology, Inc. has 9 FDA 510(k) cleared medical devices. Based in Lavergne, US.
Historical record: 9 cleared submissions from 1996 to 1997. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Contour Medical Technology, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Contour Medical Technology, Inc.
9 devices
Cleared
Mar 06, 1997
QUANTUM EDGE PEDIATRIC DEFIRBRILLATION ELECTRODES
Cardiovascular
31d
Cleared
Mar 04, 1997
NOAH MONITORING ELECTRODE SYSTEM
Cardiovascular
49d
Cleared
Jul 02, 1996
DISPOSABLE HYDROGEL DEFIBRILLATION ELECTRODE/PAD
Cardiovascular
160d
Cleared
Apr 04, 1996
TEMPERATURE PROBE-TP150
General Hospital
290d
Cleared
Apr 04, 1996
TEMPERATURE PROBE-TP250
General Hospital
290d
Cleared
Apr 04, 1996
TEMPERATURE PROBE-TP350
General Hospital
290d
Cleared
Apr 04, 1996
TEMPERATURE PROBE-TP450
General Hospital
290d
Cleared
Apr 04, 1996
TEMPERATURE PROBE-TP550
General Hospital
290d
Cleared
Apr 04, 1996
TEMPERATURE PROBE-TP650
General Hospital
290d