Pharmaceutical companyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Bristol-Myers SquibbLabelled 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. See the Bristol Myers Squibb group view.
As of Nov 15, 2026, FDA's public records list Squibb & Sons with 5 510(k) clearances. The most recent is a 510(k) clearance dated May 14, 1982: TSH-SQUIBB RADIOIMMUNOASSAY KIT.
| May 14, 1982 | TSH-SQUIBB RADIOIMMUNOASSAY KITK821174 · JLW | 510(k) clearances |
| Jul 21, 1980 | ESTRIOL RIA KIT FOR USE WITH GAMMAFLOK801424 · CGI | 510(k) clearances |
| May 8, 1980 | STOMAHESIVE STERILE WAFERK800750 · EXB | 510(k) clearances |
| Apr 28, 1977 | RIA KIT, T4 CLASPK770726 · CDX | 510(k) clearances |
| Dec 30, 1976 | ANGIOTENSIN I IMMUTOPE KITK761267 · CIB | 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
