Robert Bosch Corp. is one of 14245 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Robert Bosch Corp. - FDA 510(k) Cleared Devices
Recent clearances: ERG 550 ERGOMETER BICYCLE, ERG 551 ERGOMETER, BICYCLE, ERG 555 COUCH ERGOMETER
21
Total
18
Cleared
0
Denied
Robert Bosch Corp. has 18 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 18 cleared submissions from 1979 to 1986.
Browse the FDA 510(k) cleared devices submitted by Robert Bosch Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Robert Bosch Corp.
21 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
Mar 28, 1986
HV-4
Physical Medicine
242d
Cleared
Mar 28, 1986
SP 4
Physical Medicine
214d
Cleared
Jan 16, 1986
HEARING AID ANALYSIS SYSTEM
Ear, Nose, Throat
164d
Cleared
Aug 29, 1985
DEFI 502
Cardiovascular
136d
Cleared
Aug 19, 1985
ECS 502
Cardiovascular
549d
Cleared
Jul 17, 1985
SONOMED 4
Physical Medicine
93d
Cleared
Apr 09, 1985
BOSCH IN THE EAR HEARING AID SUPERSTAR
Ear, Nose, Throat
81d
Cleared
Mar 27, 1985
POST AURICULAR HEARING AIDS STAR 33PP, 44,55F &
Gastroenterology & Urology
68d
Cleared
Mar 25, 1985
BODY HEARING AIDS MT 80 SP
Ear, Nose, Throat
66d