FDA 510(k) Applications Submitted by MICHAEL J MCGOWAN

FDA 510(k) Number Submission Date Device Name Applicant
K032703 09/02/2003 INNOVATECH STRAIGHT LASER PROBE, MODEL 420-10 INNOVATECH SURGICAL INC.
K032704 09/02/2003 INNOVATECH ILLUMINATING LASER PROBE, MODEL 420-30 INNOVATECH SURGICAL INC.


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