510(k) K163179 ยท GBM Catheter, Urethral
Onli Intermittent Catheter
| Applicant | Hollister Incorporated, Libertyville IL, US |
| Decision | Substantially Equivalent, Jan 26, 2017 |
| Received | Nov 14, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K163179
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.