510(k) K954437 ยท GKP Instrument, Coagulation, Automated
THROMBELASTOGRAPH COAGULATION ANALYZER 3000S
| Applicant | Haemoscope Corp., Skokie IL, US |
| Decision | Substantially Equivalent, Jan 30, 1996 |
| Received | Sep 22, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954437
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.