FDA 510(k) Applications Submitted by PRECISION THERAPY INTL., INC.

FDA 510(k) Number Submission Date Device Name Applicant
K992864 08/25/1999 RENDER-PLAN 3-D PRECISION THERAPY INTL., INC.
K002240 07/24/2000 RENDER-PLAN 3-D 4.00 & PRECISE-PLAN 1.0 PRECISION THERAPY INTL., INC.
K022411 07/24/2002 PRECISEPLAN 2.0 PRECISION THERAPY INTL., INC.


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