510(k) K192577 ยท GBM Catheter, Urethral
Actreen Hi-Lite Intermittent Urinary Catheters
| Applicant | B.Braun Medical, Inc., Allentown PA, US |
| Decision | Substantially Equivalent, May 7, 2020 |
| Received | Sep 19, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K192577
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.