510(k) K924124 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
BEHRING FIBRINTIMER A
| Applicant | Behring Diagnostics, Inc., Somerville NJ, US |
| Decision | Substantially Equivalent, Dec 1, 1992 |
| Received | Aug 17, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924124
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.