510(k) K202112 ยท PZL Extracorporeal Shock Wave Device For Treatment Of Diabetic Foot Ulcers
Storz Medical Duolith SD1 T-Top & Tower System with C-Actor Sepia Handpiece
| Applicant | Storz Medical AG, Tagerwilen, CH |
| Decision | Substantially Equivalent, Feb 21, 2021 |
| Received | Jul 30, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202112
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.