510(k) K061350 ยท LNS Lithotriptor, Extracorporeal Shock-Wave, Urological
LITHODIAMOND ULTRA
| Applicant | Pck Electronic Industry & Trade Co., Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Dec 22, 2006 |
| Received | May 15, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061350
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.