Robert Bosch Corp. - FDA 510(k) Cleared Devices
21
Total
18
Cleared
0
Denied
FDA 510(k) Regulatory Record - Robert Bosch Corp. Cardiovascular ✕
6 devices
Cleared
Jun 16, 1986
ERG 550 ERGOMETER BICYCLE
Cardiovascular
216d
Cleared
Jun 16, 1986
ERG 551 ERGOMETER, BICYCLE
Cardiovascular
216d
Cleared
Jun 16, 1986
ERG 555 COUCH ERGOMETER
Cardiovascular
216d
Cleared
Aug 29, 1985
DEFI 502
Cardiovascular
136d
Cleared
Aug 19, 1985
ECS 502
Cardiovascular
549d
Cleared
Apr 11, 1979
TONOTEST BLOOD PRESSURE DEVICE
Cardiovascular