510(k) K981592 ยท LOQ Device, General Purpose, Hematology
ACS:CENTAUR AFP
| Applicant | Chiron Diagnostics Corp., Medfield MA, US |
| Decision | Substantially Equivalent, Jul 7, 1998 |
| Received | May 4, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981592
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.