FDA 510(k) Applications Submitted by DANIEL CONSAGA

FDA 510(k) Number Submission Date Device Name Applicant
K092488 08/13/2009 DYNAREX STERILE LUBRICATING JELLY DYNAREX CORPORATION
K102637 09/14/2010 DYNAREX ULTRASOUND GEL DYNAREX CORPORATION
K103086 10/19/2010 DYNAREX INTERMITTENT CATHETERS, MALE, FEMALE, PEDIATRIC DYNAREX CORPORATION


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