510(k) K993678 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
THROMBELASTOGRAPH COAGULATION ANALYZER TEG - 5000 SERIES
| Applicant | Haemoscope Corp., Skokie IL, US |
| Decision | Substantially Equivalent, May 5, 2000 |
| Received | Nov 1, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993678
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.