510(k) K062081 ยท LNS Lithotriptor, Extracorporeal Shock-Wave, Urological
LITHOGOLD
| Applicant | Tissue Regeneration Technologies, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Nov 2, 2006 |
| Received | Jul 21, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062081
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.