510(k) K072788 ยท LNS Lithotriptor, Extracorporeal Shock-Wave, Urological
STORZ MODULITH LITHOTRIPTER SLX-F2-F180
| Applicant | KARL STORZ Endoscopy-America, Inc., Culver City CA, US |
| Decision | Substantially Equivalent, Dec 26, 2007 |
| Received | Oct 1, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072788
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.