510(k) K181206 ยท GBM Catheter, Urethral
GentleCath Glide Intermittent Urinary Catheter
| Applicant | Convatec Limited, Deeside, GB |
| Decision | Substantially Equivalent, Aug 16, 2018 |
| Received | May 7, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181206
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.