510(k) K193041 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
Hemochron Signature Elite
| Applicant | Accriva Diagnostics, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Nov 22, 2019 |
| Received | Oct 31, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K193041
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.