510(k) K924393 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
STANDARD HUMAN PLASMA
| Applicant | Behring Diagnostics, Inc., Somerville NJ, US |
| Decision | Substantially Equivalent, Nov 16, 1992 |
| Received | Aug 31, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924393
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.