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., part of HaemoneticsLabelled 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 Haemoscope Corp. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jan 31, 2007: RAPIDTEG TEG-ACT TEST.
| Jan 31, 2007 | RAPIDTEG TEG-ACT TESTK062604 · JBP | 510(k) clearances |
| Sep 1, 2004 | THROMBELASTOGRAPH (TEG) PLATELET MAPPING ASSAYK041502 · JOZ | 510(k) clearances |
| Sep 14, 2000 | THROMBELASTOGRAPH COAGULATION ANALYZER TEG-5000 SERIESK002177 · JPA | 510(k) clearances |
| May 5, 2000 | THROMBELASTOGRAPH COAGULATION ANALYZER TEG - 5000 SERIESK993678 · JPA | 510(k) clearances |
| Jan 30, 1996 | THROMBELASTOGRAPH COAGULATION ANALYZER 3000SK954437 · GKP | 510(k) clearances |
| Nov 1, 1990 | THROMBELASTOGRAPHK904204 · GKP | 510(k) clearances |
| Oct 24, 1989 | THROMBELASTOGRAPH(R)K895844 · GKP | 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
