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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