510(k) K212301 ยท LFL Instrument, Ultrasonic Surgical
Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device
| Applicant | Covidien, LLC, Boulder CO, US |
| Decision | Substantially Equivalent, Nov 15, 2021 |
| Received | Jul 23, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212301
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.