510(k) K012482 ยท LNS Lithotriptor, Extracorporeal Shock-Wave, Urological
STORZ MODULITH SLK LITHOTRIPTER WITH MULTIVIEW OPTION
| Applicant | KARL STORZ Endoscopy-America, Inc., Culver City CA, US |
| Decision | Substantially Equivalent, Oct 16, 2001 |
| Received | Aug 2, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012482
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.