510(k) K193148 ยท GBM Catheter, Urethral
VaPro Plus Pocket, VaPro Plus
| Applicant | Hollister Incorporated, Libertyville IL, US |
| Decision | Substantially Equivalent, Dec 13, 2019 |
| Received | Nov 13, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K193148
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.