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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