510(k) K994208 ยท DTM Filter, Blood, Cardiopulmonary Bypass, Arterial Line
AFFINITY 20 MICRON ARTERIAL BLOOD FILTER, MODEL 353/354
| Applicant | Medtronic Perfusion Systems, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jan 13, 2000 |
| Received | Dec 14, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K994208
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.