510(k) K170422 ยท FAD Stent, Ureteral
BIOSOFT DUO DOUBLE LOOP URETERAL STENTS
| Applicant | Coloplast Corp., Plymouth MN, US |
| Decision | Substantially Equivalent, Nov 2, 2017 |
| Received | Feb 13, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170422
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.