510(k) K101797 ยท LFL Instrument, Ultrasonic Surgical
SONICISION CORDLESS ULTRASONIC DISSECTION DEVICE MODEL SCD391, SCD396, SCT12, SCG, SCB, SCSK, SONICISION STERILIZATION T
| Applicant | Covidien, Formerly Valleylab, A Division of Tyco, Boulder CO, US |
| Decision | Substantially Equivalent, Feb 24, 2011 |
| Received | Jun 28, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101797
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.