510(k) K002929 ยท LNS Lithotriptor, Extracorporeal Shock-Wave, Urological
DORNIER COMPACT ALPHA LITHOTRIPTER
| Applicant | Dornier Medtech America, Inc., Kennesaw GA, US |
| Decision | Substantially Equivalent, Apr 17, 2001 |
| Received | Sep 20, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002929
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.