510(k) K190312 ยท FAD Stent, Ureteral
Dornier Ureteral Stent
| Applicant | Dornier Medtech America, Inc., Kennesaw GA, US |
| Decision | Substantially Equivalent, Nov 15, 2019 |
| Received | Feb 12, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190312
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.