510(k) K180801 ยท GBM Catheter, Urethral
Actreen Hi-Lite Cath, Actreen Hi-Lite Set
| Applicant | B.Braun Medical, Inc., Allentown PA, US |
| Decision | Substantially Equivalent, Nov 5, 2018 |
| Received | Mar 28, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180801
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.