510(k) K926551 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
BEHRING FIBRINTIMER A
| Applicant | Behring Diagnostics, Inc., Westwood MA, US |
| Decision | Substantially Equivalent, Apr 18, 1995 |
| Received | Dec 31, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926551
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.