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FDA 510(k) Applications Submitted by DAVID K QUON, M.D.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K061850
06/30/2006
MINI-YAG LASER
AMERICAN LASERS, INC.
K974142
11/03/1997
HM-RUBY
AMERICAN LASERS, INC.
K970475
02/07/1997
MM-RUBY
AMERICAN LASERS, INC.
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