510(k) K191143 ยท PTD Subcutaneous Implanted Apheresis Port
PowerFlow Implantable Apheresis IV Port
| Applicant | C.R. Bard, Inc., Salt Lake Ciy, UT, US |
| Decision | Substantially Equivalent, Aug 2, 2019 |
| Received | Apr 30, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191143
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.