Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Tracor Northern with 10 510(k) clearances. The most recent is a 510(k) clearance dated Dec 29, 1988: NEURAL MAGNETIC STIMULATOR, THE D190.
| Dec 29, 1988 | NEURAL MAGNETIC STIMULATOR, THE D190K883340 · GWF | 510(k) clearances |
| Feb 29, 1988 | GUARDIAN, EEG BRAIN MONITORING SYSTEMK874733 · OLT | 510(k) clearances |
| Aug 18, 1986 | TM-3400, NOMAD (MODIFIED)K860968 · GWF | 510(k) clearances |
| Jun 5, 1986 | TM-3600 A NEURODIAGNOSTIC SYSTEMK860903 · GWF | 510(k) clearances |
| Aug 16, 1985 | CDSA(COLOR DENSITY, SPECTRAL ARRRAY)K852587 · OLT | 510(k) clearances |
| Jun 4, 1985 | NOMAD TM-3400K850109 · GWF | 510(k) clearances |
| Dec 28, 1984 | PHOTIC STIMULATOR TM-3030-70K842964 · GWE | 510(k) clearances |
| Aug 16, 1983 | EVOKED 3500 POTENTIAL SYSTEMK832084 · GWE | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
