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 14, 2026, FDA's public records list In Vitro Technologies with 7 510(k) clearances. The most recent is a 510(k) clearance dated Sep 14, 1992: 866.5750 RADIOALLERGOSORBENT IMMUNLOGICAL TEST SYS.
| Sep 14, 1992 | 866.5750 RADIOALLERGOSORBENT IMMUNLOGICAL TEST SYSK914685 · DHB | 510(k) clearances |
| Nov 29, 1990 | IVT RAST TRACERK904661 · DHB | 510(k) clearances |
| Apr 7, 1988 | IVT CENTRAL ALLERGY SCREENK875329 · DHB | 510(k) clearances |
| Mar 23, 1988 | IVT WESTERN ALLERGY SCREENK875328 · DHB | 510(k) clearances |
| Jan 11, 1988 | IVT SOUTHEAST ALLERGY SCREENK874168 · DHB | 510(k) clearances |
| Jan 11, 1988 | IVT NORTHEAST ALLERGY SCREENK874169 · DHB | 510(k) clearances |
| May 1, 1987 | IVT SOUTHWEST ALLERGY SCREENK870625 · DHB | 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
