510(k) K880671 ยท DTM Filter, Blood, Cardiopulmonary Bypass, Arterial Line
MODIFIED INTERSEPT PEDIATRIC BLOOD FILTER
| Applicant | Medtronic Blood Systems, Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, May 6, 1988 |
| Received | Feb 18, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880671
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.