FDA 510(k) Applications Submitted by JENNIFER SULLIVAN

FDA 510(k) Number Submission Date Device Name Applicant
K120944 03/29/2012 KENDALL SCD 700 SEQUENTIAL COMPRESSION CONTROLLER COVIDIEN
K130904 04/01/2013 TRELLIS-8 PERIPHERAL INFUSION SYSTEM COVIDIEN
K091378 05/11/2009 MAMMOSITE II RADIATION THERAPY SYSTEM HOLOGIC, INC.
K092405 08/06/2009 MAMMOSITE MULTI LUMEN HOLOGIC, INC.
K123196 10/11/2012 PALINDROME PRECISION H CHRONIC CATHETER, PALINDROME PRECISION SI CHRONIC CATHETER, PALINDROME PRECISION HSI CHRONIC CATH COVIDIEN
K163055 11/01/2016 Reprocessed Kendall SCD Express Foot Cuff COVIDIEN


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