510(k) K150935 ยท GBM Catheter, Urethral
SpeediCath Compact Eve
| Applicant | Coloplast A/S, Plymouth MN, US |
| Decision | Substantially Equivalent, Jul 2, 2015 |
| Received | Apr 7, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150935
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.