510(k) K172333 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
Sysmex CS-5100
| Applicant | Siemens Healthcare Diagnostics Products GmbH, Marburg, DE |
| Decision | Substantially Equivalent, Oct 31, 2017 |
| Received | Aug 2, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172333
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.