FDA 510(k) Applications Submitted by MARK MOYER

FDA 510(k) Number Submission Date Device Name Applicant
K020079 01/10/2002 BLADEWORKS MICROKERATOME BLADE, MODEL 7061 BLADE WORKS, INC.
K022716 08/15/2002 MED-LOGICS MICROKERATOME BLADE, MODEL 7020CLB MED-LOGICS, INC.
K022982 09/09/2002 MED-LOGICS MICROKERATOME BLADE, MODEL 7050CLB MED-LOGICS, INC.


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