FDA 510(k) Applications Submitted by COVIDIEN, FORMERLY VALLEYLAB, A DIVISION OF TYCO
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K101797 | 06/28/2010 | SONICISION CORDLESS ULTRASONIC DISSECTION DEVICE MODEL SCD391, SCD396, SCT12, SCG, SCB, SCSK, SONICISION STERILIZATION T | COVIDIEN, FORMERLY VALLEYLAB, A DIVISION OF TYCO |
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