FDA 510(k) Applications Submitted by LEE BUI

FDA 510(k) Number Submission Date Device Name Applicant
K000124 01/18/2000 SENSATION -VACUUM ASSIST DEVICES PROSURG, INC.
K001576 05/22/2000 EVA -VACUUM ASSIST DEVICE FOR CLITORAL THERAPY PROSURG, INC.
K994151 12/09/1999 PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES XIMED/PROSURE/INJECTX


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