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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