510(k) K940840 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
ACT CONTROL SET
| Applicant | Sigma Diagnostics, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Jul 19, 1994 |
| Received | Feb 23, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940840
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.