510(k) K110862 ยท GBM Catheter, Urethral
VAPRO PLUS INTERMITTENT CATHETER
| Applicant | Hollister Incorporated, Libertyville IL, US |
| Decision | Substantially Equivalent, Apr 26, 2011 |
| Received | Mar 29, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K110862
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.