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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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