510(k) K033137 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
POTENS +
| Applicant | Wada, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Dec 8, 2003 |
| Received | Sep 30, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033137
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.