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FDA 510(k) Applications Submitted by ROBERT BOVY
FDA 510(k) Number
Submission Date
Device Name
Applicant
K130605
03/07/2013
INOMAX DSIR (DELIVERY SYSTEM)
INO THERAPEUTICS
K131686
06/10/2013
INOMAX DSIR (DELIVERY SYSTEM)
INO THERAPEUTICS/IKARIA
K082005
07/14/2008
MODIFICATION TO HI-ART TREATMENT SYSTEM
TOMOTHERAPY INCORPORATED
K122689
09/04/2012
INOBLENDER
INO THERAPEUTICS
K143213
11/10/2014
INOmax DSIR Plus MRI
INO Therapeutics/Ikaria
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