Bosch Hearing Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bosch Hearing Instruments, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Bosch Hearing Instruments, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1980 to 1985. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Bosch Hearing Instruments, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bosch Hearing Instruments, Inc.
7 devices
Cleared
Dec 30, 1985
EKG 501 A
Cardiovascular
691d
Cleared
Dec 30, 1985
EKG 503A
Cardiovascular
691d
Cleared
Nov 14, 1985
EBM-500
Cardiovascular
645d
Cleared
Sep 30, 1982
BOSCH STAR 66F-SP HEARING AID
Ear, Nose, Throat
36d
Cleared
Jan 22, 1982
BOSCH TOP STAR III
Ear, Nose, Throat
15d
Cleared
Mar 31, 1981
BOSCH STAR 66F SUPER EARLEVEL AID
Ear, Nose, Throat
49d
Cleared
Jun 04, 1980
OMNITON MT80-A BODY HEARING AID
Ear, Nose, Throat
57d