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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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