510(k) K832225 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
ORTHO ABNORMAL COAGULATION LEVEL I/II
| Applicant | Ortho Diagnostic Systems, Inc., Carpinteria CA, US |
| Decision | Substantially Equivalent, Aug 12, 1983 |
| Received | Jul 8, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832225
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.