Diagnostics 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 Life Science Instrumentation with 20 510(k) clearances. The most recent is a 510(k) clearance dated Nov 5, 1985: EMERGIPACE - EXTERNAL PACEMAKER.
| Nov 5, 1985 | EMERGIPACE - EXTERNAL PACEMAKERK850812 · DRO | 510(k) clearances |
| Mar 1, 1985 | LS 5K842037 · DRT | 510(k) clearances |
| Oct 19, 1984 | LS-260G MONITOR/RECORDER & DEFIBILLATORK843396 · LDD | 510(k) clearances |
| Apr 17, 1984 | MINI-DEFIBRILLATOR 280/4K840246 · LDD | 510(k) clearances |
| Apr 28, 1983 | DEFIBRILLATOR VPD 545K831056 · LDD | 510(k) clearances |
| Apr 28, 1983 | VPD540 DEFIBRILLATORK822617 · LDD | 510(k) clearances |
| Oct 18, 1982 | LS6 ARRYTHMIA DISCRIMINATORK822616 · DSI | 510(k) clearances |
| Sep 21, 1982 | LIFE WATCH LSIK822615 · 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
