Medical device makerLabelled 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 13, 2026, FDA's public records list Litton Datamedix with 5 510(k) clearances. The most recent is a 510(k) clearance dated Mar 21, 1986: LITTON DATAMEDIX BLOOD PRESSURE MONITOR NI.
| Date | Record | Source |
|---|---|---|
| Mar 21, 1986 | LITTON DATAMEDIX BLOOD PRESSURE MONITOR NIK853599 · DXN | 510(k) clearances |
| Apr 18, 1985 | ULTRASOUND GELK850290 · IYO | 510(k) clearances |
| Oct 4, 1984 | SERVOMED OXYMONITO SMK 363K842497 · KLK | 510(k) clearances |
| Aug 27, 1984 | SERVOCARD DEFIBRILLATOR SCP-851K842235 · LDD | 510(k) clearances |
| Aug 27, 1984 | SERVOCARD SCP-840K842312 · LDD | 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
