510(k) K153371 ยท LFL Instrument, Ultrasonic Surgical
Sonicision Cordless Ultrasonic Dissection Device
| Applicant | Covidien, LLC, Boulder CO, US |
| Decision | Substantially Equivalent, Mar 28, 2016 |
| Received | Nov 23, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153371
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.