510(k) K190659 ยท FAD Stent, Ureteral
Ureteral Stent Open Tip/Closed Tip/Intraoperative Tip, Ureteral Stent via Ureterorenoscope Open Tip/Closed Tip, Pediatric Ureteral Stent Open Tip/Closed Tip, Mono J Urinary Diversion Ureteral Stent Open Tip/Closed Tip, Multiloop Ureteral Stent Open Tip/Closed Tip
| Applicant | Allwin Medical Devices, Inc., Anaheim CA, US |
| Decision | Unknown, Dec 2, 2019 |
| Received | Mar 14, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190659
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.