Tracor Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tracor Instruments, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Tracor Instruments, Inc. has 10 FDA 510(k) cleared ear, nose, throat devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1976 to 1985.
Browse the complete list of FDA 510(k) cleared ear, nose, throat devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tracor Instruments, Inc.
10 devices
Cleared
Oct 16, 1985
TRACOR MODEL RA600 MICROPROCESSOR AUDIOMETER
Ear, Nose, Throat
76d
Cleared
Jun 20, 1985
TRACOR 200 MICROPROCESSOR AUDIOMETER/TRACOR RA 200
Ear, Nose, Throat
72d
Cleared
Aug 30, 1982
TRACOR RA400 AUDIOMETER
Ear, Nose, Throat
19d
Cleared
May 31, 1979
TRACOR MODEL RA-411 MICROPROCESSOR
Ear, Nose, Throat
20d
Cleared
Dec 01, 1978
STIMULATOR, TN-3001 SOMATOSENSORY
Neurology
52d
Cleared
Dec 01, 1978
RESPONSE SYSTEM, TN-3000
Neurology
42d
Cleared
May 16, 1978
SPEECH AUDIOMETER RA 226
Ear, Nose, Throat
12d
Cleared
Mar 30, 1978
TRACOR RA 410 AUDIOMETER
Ear, Nose, Throat
10d
Cleared
Mar 30, 1978
AUDIOMETER CALIBRATOR MODEL RA 310
Ear, Nose, Throat
6d
Cleared
Oct 29, 1976
TRACOR MODEL RA 208 COMPLIANCE AUDIOM
Ear, Nose, Throat
11d