510(k) K892387 ยท DTM Filter, Blood, Cardiopulmonary Bypass, Arterial Line
MODIFIED GELMAN ARTERIAL FILTER
| Applicant | Gelman Sciences, Inc., Ann Arbor MI, US |
| Decision | Substantially Equivalent, Jun 22, 1989 |
| Received | Apr 14, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892387
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.