510(k) K883635 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
KD 0.1 M SODIUM CITRATE SOLUTION
| Applicant | King Diagnostics, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Oct 31, 1988 |
| Received | Aug 25, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883635
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.