510(k) K172084 ยท LNS Lithotriptor, Extracorporeal Shock-Wave, Urological
Delta III Lithotripter
| Applicant | Dornier Medtech America, Inc., Kennesaw GA, US |
| Decision | Substantially Equivalent, Aug 8, 2017 |
| Received | Jul 10, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K172084
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.