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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K101797

SONICISION CORDLESS ULTRASONIC DISSECTION DEVICE MODEL SCD391, SCD396, SCT12, SCG, SCB, SCSK, SONICISION STERILIZATION T · Covidien, Formerly Valleylab, A Division of Tyco · decided 2011-02-24 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
SonicisionSCD396Covidien LPLFL20884521052663
SonicisionSCGCovidien LPLFL10884521036536
SonicisionSCD391Covidien LPLFL10884521052659
SonicisionSCT12Covidien LPLFL10884524002958
Battery ChargerCBCCovidien LPLFL10884521037212
SonicisionSCD391Covidien LPLFL10884521807860
SonicisionSCD396Covidien LPLFL10884521807877