510(k) K895844 ยท GKP Instrument, Coagulation, Automated
THROMBELASTOGRAPH(R)
| Applicant | Haemoscope Corp., Morton Grove IL, US |
| Decision | Substantially Equivalent, Oct 24, 1989 |
| Received | Oct 3, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895844
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.