510(k) K212049 ยท LFL Instrument, Ultrasonic Surgical
Oclet TDS 1000
| Applicant | Tendonova Corporation, Norcross GA, US |
| Decision | Substantially Equivalent, Mar 8, 2022 |
| Received | Jun 30, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212049
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.