510(k) K161672 ยท GBM Catheter, Urethral
SpeediCath Flex Coude
| Applicant | Coloplast Corp., Plymouth MN, US |
| Decision | Substantially Equivalent, Sep 29, 2016 |
| Received | Jun 9, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161672
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.