510(k) K072538 ยท LNS Lithotriptor, Extracorporeal Shock-Wave, Urological
PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPTER
| Applicant | United Medical Systems, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jan 30, 2008 |
| Received | Sep 7, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072538
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.