FDA 510(k) Applications Submitted by DAVID M HORTON

FDA 510(k) Number Submission Date Device Name Applicant
K131170 04/24/2013 SONICISION STERILIZATION TRAY COVIDIEN, FORMERLY VALLEYLAB, A DIVISION OF TYCO H
K141371 05/27/2014 SONICISION CORDLESS ULTRASONIC DISSECTOR COVIDIEN, FORMERLY VALLEYLAB, A DIVISION OF TYCO H
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
K102470 08/30/2010 LUGASURE CURVED, SMALL JAW, OPEN SEALER/DIVIDER COVIDIEN, FORMERLY VALLEYLAB,
K112536 09/01/2011 SONICISION STERILIZATION TRAY COVIDIEN


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