510(k) K213772 ยท LNS Lithotriptor, Extracorporeal Shock-Wave, Urological
LM-9300 Plus Lithotripter
| Applicant | Lite-Med, Inc., Taipei, TW |
| Decision | Substantially Equivalent, Jan 19, 2023 |
| Received | Dec 2, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213772
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.