Diagnostics makerLabelled 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.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Universal Reagents with 8 510(k) clearances. The most recent is a 510(k) clearance dated Sep 25, 1997: UNIVERSAL REAGENT FACTOR XII (TWELVE) DEFICIENT PLASMA.
| Date | Record | Source |
|---|---|---|
| Sep 25, 1997 | UNIVERSAL REAGENT FACTOR XII (TWELVE) DEFICIENT PLASMAK973143 · GGP | 510(k) clearances |
| Jul 14, 1997 | FACTOR DEFICIENT PLASMAS - FACTOR IX (9)K972288 · GGP | 510(k) clearances |
| Jul 14, 1997 | FACTOR DEFICIENT PLASMAS - FACTOR XI (11)K972286 · GJT | 510(k) clearances |
| Apr 25, 1997 | UNIVERSAL REAGENT FACTOR VII DEFICIENT PLASMAK970607 · GJT | 510(k) clearances |
| Apr 25, 1997 | UNIVERSAL REAGENT FACTOR VIII DEFICIENT PLASMAK970593 · GJT | 510(k) clearances |
| Dec 18, 1996 | UNIVERSAL REAGENT FACTOR V DEFICIENT PLASMAK964270 · GGP | 510(k) clearances |
| Dec 18, 1996 | UNIVERSAL REAGENT FACTOR X DEFICIENT PLASMAK964459 · GGP | 510(k) clearances |
| Oct 10, 1996 | FACTOR DEFICIENT PLASMAK961929 · GGP | 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
