510(k) K170583 ยท DTN Reservoir, Blood, Cardiopulmonary Bypass
Intersept Filtered Cardiotomy Reservoir with Cortiva BioActive Surface
| Applicant | Medtronic, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Mar 17, 2017 |
| Received | Feb 28, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K170583
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.