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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