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 American Surgical Instruments with 6 510(k) clearances. The most recent is a 510(k) clearance dated Nov 8, 1993: DISPOSABLE UNIPOLAR COAGULATOR PROBE SYSTEM.
| Nov 8, 1993 | DISPOSABLE UNIPOLAR COAGULATOR PROBE SYSTEMK921716 · HET | 510(k) clearances |
| May 13, 1993 | IRRIGATION PUMPS AND TUBING AND SUCTION TUBINGK921457 · GCJ | 510(k) clearances |
| Mar 9, 1992 | NEZHAT/DORSEY HYDRO DISSECTION PUMP & ACCESSORIESK913944 · HET | 510(k) clearances |
| Nov 1, 1991 | NEZHAT DORSEY SUCTION PROBE W/INNER IRRIGA TUBEK913999 · GCJ | 510(k) clearances |
| Jun 20, 1991 | UNIPOLAR COAGULATOR PROBE SYSTEMK911274 · GEI | 510(k) clearances |
| Mar 28, 1990 | NEZHAT/DORSEY HYDRO DISSECTION PUMP OB-GYN USEK896118 · HET | 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
