510(k) K183390 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
QNext and DG-PT
| Applicant | Diagnostic Grifols, S.A., Partes Del Valles, ES |
| Decision | Substantially Equivalent, Aug 21, 2019 |
| Received | Dec 6, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183390
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.