510(k) K070799 ยท LNS Lithotriptor, Extracorporeal Shock-Wave, Urological
MODULARIS VARIOSTAR
| Applicant | Siemens Medical Solutions USA, Inc., Malvern PA, US |
| Decision | Substantially Equivalent, Nov 1, 2007 |
| Received | Mar 23, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070799
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 24, 2015 | Siemens Medical Solutions USA, Inc MODULARIS VARIOSTAR; Lithotripter device designed to treat urolithiasis. Terminated |
LNS | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.