510(k) K062147 ยท LNS Lithotriptor, Extracorporeal Shock-Wave, Urological
INTEGRA SL
| Applicant | Direx Systems Corp., Canton MA, US |
| Decision | Substantially Equivalent, Oct 20, 2006 |
| Received | Jul 27, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062147
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.