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 15, 2026, FDA's public records list Litton Medical Electronics with 38 510(k) clearances. The most recent is a 510(k) clearance dated May 16, 1985: RECOMED BLOOD-FLOW METER H236-052-02.
| May 16, 1985 | RECOMED BLOOD-FLOW METER H236-052-02K840522 · DPW | 510(k) clearances |
| Nov 20, 1984 | SERVOMED ARRHYCOMP CENTRAL MONITOR SYSK840899 · DSI | 510(k) clearances |
| Nov 20, 1984 | RECOMED CARDIAC OUTPUT METER 236067-K840439 · DXG | 510(k) clearances |
| Oct 29, 1984 | SERVOMED PULSE AMPLIFIER MODULE-206-K840523 · DRT | 510(k) clearances |
| Oct 26, 1984 | SERVOMED BASIC BEDSIDE UNIT SMV 110TPK840524 · DRT | 510(k) clearances |
| Sep 20, 1984 | SERVOMED MEDIVISION SCOPE SMV-235K840209 · DXJ | 510(k) clearances |
| Sep 20, 1984 | SERVOMED OXCARDIORE SPIROGRAPH 324/111K840832 · DRT | 510(k) clearances |
| Jun 1, 1984 | SERVOMED DIGITAL DISPLAY MODULEK840521 · DRT | 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
