510(k) K000053 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
ACL 9000 SYSTEM
| Applicant | Instrumentation Laboratory CO, Bedford MA, US |
| Decision | Substantially Equivalent, Mar 15, 2000 |
| Received | Jan 7, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000053
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.