510(k) K141642 ยท GBM Catheter, Urethral
VAPRO INTERMITTENT CATHETER
| Applicant | Hollister Incorporated, Libertyville IL, US |
| Decision | Substantially Equivalent, Aug 22, 2014 |
| Received | Jun 19, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K141642
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.