510(k) K090960 ยท GBM Catheter, Urethral
VAPRO INTERMITTENT CATHETER, MODEL 72062, 72082,72102, 72122, 72142, 72064, 72084, 72104, 72124,72144, 72164, 72184,
| Applicant | Hollister, Inc., Libertyville IL, US |
| Decision | Substantially Equivalent, Aug 20, 2009 |
| Received | Apr 6, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090960
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.