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FDA 510(k) Applications Submitted by DAVID DOWNEY
FDA 510(k) Number
Submission Date
Device Name
Applicant
K960765
02/26/1996
MENTOR ADVENT A/B SYSTEM
MENTOR OPHTHALMICS, INC.
K971538
04/28/1997
MENTOR GEMINI HEMOSTATIC ERASER
MENTOR OPHTHALMICS, INC.
K964312
10/29/1996
MENTOR TONO-PEN 3
MENTOR OPHTHALMICS, INC.
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