510(k) K183253 ยท GBM Catheter, Urethral
ValPro 2 Plus, VaPro 2 Plus Pocket
| Applicant | Hollister Incorporated, Libertyville IL, US |
| Decision | Substantially Equivalent, Dec 18, 2018 |
| Received | Nov 21, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K183253
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.