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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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