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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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