510(k) K180824 ยท GBM Catheter, Urethral
VaPro 2 Intermittent Catheter
| Applicant | Hollister Incorporated, Libertyville IL, US |
| Decision | Substantially Equivalent, Jun 22, 2018 |
| Received | Mar 30, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K180824
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.