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FDA 510(k) Applications Submitted by REFRACTEC, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K053475
12/14/2005
OPTIPOINT CORNEAL MARKER, MODEL VPT-OPT-450
REFRACTEC, INC.
K980522
02/10/1998
REFRACTEC MCS-100
REFRACTEC, INC.
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