Tracor Northern, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tracor Northern, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Tracor Northern, Inc. has 10 FDA 510(k) cleared neurology devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1981 to 1988.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tracor Northern, Inc.
10 devices
Cleared
Dec 29, 1988
NEURAL MAGNETIC STIMULATOR, THE D190
Neurology
142d
Cleared
Feb 29, 1988
GUARDIAN, EEG BRAIN MONITORING SYSTEM
Neurology
103d
Cleared
Aug 18, 1986
TM-3400, NOMAD (MODIFIED)
Neurology
160d
Cleared
Jun 05, 1986
TM-3600 A NEURODIAGNOSTIC SYSTEM
Neurology
87d
Cleared
Aug 16, 1985
CDSA(COLOR DENSITY, SPECTRAL ARRRAY)
Neurology
59d
Cleared
Jun 04, 1985
NOMAD TM-3400
Neurology
141d
Cleared
Dec 28, 1984
PHOTIC STIMULATOR TM-3030-70
Neurology
154d
Cleared
Aug 16, 1983
EVOKED 3500 POTENTIAL SYSTEM
Neurology
49d
Cleared
Sep 24, 1982
THE 3500
Neurology
45d
Cleared
Mar 17, 1981
TN-3000 EVOKED RESPONSE SYSTEM
Neurology
14d