510(k) K242254 · PNO Catheter, Percutaneous, Cutting/Scoring
D·Kutting LL Peripheral Scoring Balloon Dilatation Catheter
| Applicant | Dk Medical Technology Co., Ltd., Jiangsu, CN |
| Decision | Substantially Equivalent, Apr 21, 2025 |
| Received | Jul 31, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242254
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.