510(k) K011873 ยท LNS Lithotriptor, Extracorporeal Shock-Wave, Urological
DORNIER LITHOTRIPTER S(DOLI S) & DORNIER LITHOTRIPTER S-XP (DOLI S-XP)
| Applicant | Dornier, Kennesaw GA, US |
| Decision | Substantially Equivalent, Aug 31, 2001 |
| Received | Jun 15, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011873
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.