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FDA 510(k) Applications Submitted by YMED INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K082343
08/15/2008
VASCUTRAK 2, MODELS: V14 AND V18
YMED INC.
K063657
12/08/2006
VASCUTRAK PTA DILATION CATHETER
YMED INC.
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