510(k) K213978 ยท HRX Arthroscope
TELIGEN System
| Applicant | Medos International SARL, Lelocle, CH |
| Decision | Substantially Equivalent, Oct 18, 2022 |
| Received | Dec 20, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213978
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.