510(k) K143182 ยท GBM Catheter, Urethral
Speedicath Compact Male
| Applicant | Coloplast A/S, Plymouth MN, US |
| Decision | Substantially Equivalent, Jan 20, 2015 |
| Received | Nov 5, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143182
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.