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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