510(k) K242922 ยท LNS Lithotriptor, Extracorporeal Shock-Wave, Urological
Extracorporeal Shock Wave Lithotripter (U200)
| Applicant | Shenzhen Wikkon Precision Technologies Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Jun 18, 2025 |
| Received | Sep 24, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242922
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.