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 Gamp & Assoc. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jan 5, 1996: GAMP & ASSOCIATES DISPOSABLE END IRRIGATING ENDOILLUMINATOR.
| Jan 5, 1996 | GAMP & ASSOCIATES DISPOSABLE END IRRIGATING ENDOILLUMINATORK952585 · MPA | 510(k) clearances |
| Jan 5, 1996 | GAMP & ASSOCIATES DISPOSABLE FIBEROPTIC VISCOINJECTORK952581 · MPA | 510(k) clearances |
| Jan 5, 1996 | GAMP & ASSOCIATES THREE FUNCTION DISPOSABLE MANIPULATORK952569 · HQR | 510(k) clearances |
| Dec 22, 1995 | GAMP & ASSOC. DISPOSABLE ASPIRATING ENDOOCULAR LASER PROBEK954308 · HQB | 510(k) clearances |
| Dec 22, 1995 | GAMP & ASSOC. DISPOSABLE ILL ENDOCULAR LASER PROBEK954306 · HQB | 510(k) clearances |
| Dec 22, 1995 | GAMP & ASSOC. DISPOSABLE ENDOOCULAR LASER PROBEK954307 · HQB | 510(k) clearances |
| Sep 1, 1995 | GAMP & ASSOCIATES DISPOSABLE BARE END FIBERK952580 · MPA | 510(k) clearances |
| Sep 1, 1995 | GAMP & ASSOCIATES DISPOSABLE ENDOILLUMINATOR W/PICKK952584 · MPA | 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
