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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