510(k) K870685 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
COAGULATION CONTROL, LEVEL I
| Applicant | U. S. Diagnostics, Inc., San Luis Obispo CA, US |
| Decision | Substantially Equivalent, Apr 20, 1987 |
| Received | Feb 19, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870685
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.