510(k) K952532 ยท DTM Filter, Blood, Cardiopulmonary Bypass, Arterial Line
AFFINITY ARTERIAL BLOOD FILTER
| Applicant | Avecor Cardiovascular, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Oct 6, 1995 |
| Received | Jun 1, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952532
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 14, 2019 | Medtronic Perfusion Systems Medtronic Affinity, 38um Arterial Filter, Catalog number REF 351 Terminated |
DTM | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.