Gereonics, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Gereonics, Inc. has 4 FDA 510(k) cleared medical devices. Based in Escondido, US.
Historical record: 4 cleared submissions from 1986 to 2007. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Gereonics, Inc. Filter by specialty or product code using the sidebar.
4 devices
Cleared
Jun 13, 2007
GEREONICS ULTRA-PIEZO LIMB MOVEMENT SENSOR
Anesthesiology
260d
Cleared
Apr 28, 1999
GEREONICS ULTRA-PIEZO RESPIRATORY EFFORT SENSOR
Anesthesiology
33d
Cleared
Feb 08, 1999
GEREONICS ULTRA-PIEZO RESPIRATORY EFFORT SENSOR
Anesthesiology
131d
Cleared
Aug 06, 1986
GEREONICS BIOPOTENTIAL SKIN ELECTRODES
Cardiovascular
135d