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FDA 510(k) Applications Submitted by AMERICAN OPTISURGICAL, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K080803
03/21/2008
VISUAL PHACOEMULSIFICATION SYSTEM, MODEL 551
AMERICAN OPTISURGICAL, INC.
K101561
06/04/2010
TX1 TISSUE REMOVAL SYSTEM
AMERICAN OPTISURGICAL, INC.
K020527
02/19/2002
HORIZON PHACOEMULSIFICATION SYSTEM, MODEL HZN-2030
AMERICAN OPTISURGICAL, INC.
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