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 Argus Medical with 6 510(k) clearances. The most recent is a 510(k) clearance dated Aug 24, 1995: ARGUS HYSTEROSCOPY INSTRUMENT SYSTEM.
| Aug 24, 1995 | ARGUS HYSTEROSCOPY INSTRUMENT SYSTEMK950255 · HIH | 510(k) clearances |
| Jul 26, 1995 | ARGUS MEDICAL COMPANY LAPAROSCOPIC DISCECTOMY INSTRUMENT SYSTEMK951624 · HRX | 510(k) clearances |
| May 15, 1995 | ARGUS ARTHROSCOPY INSTRUMENT SYSTEMK950242 · HRX | 510(k) clearances |
| Mar 3, 1995 | ARGUS ENDOSCOPIC PLASTIC SURGERY INSTRUMENT SYSTEMK950297 · GCJ | 510(k) clearances |
| Feb 17, 1995 | ARGUS SINUS ENDOSCOPY INSTRUMENT SYSTEMK946011 · EOB | 510(k) clearances |
| Feb 9, 1995 | ARGUS LAPAROSCOPY INSTRUMENT SYSTEMK950378 · GCJ | 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
