FDA 510(k) Applications Submitted by MARY "PENNIE" DRINKARD

FDA 510(k) Number Submission Date Device Name Applicant
K993597 10/25/1999 PLLL, TELERADPRO, MODEL 12714/12715, VXR-12 PLUS, MODEL 8619/9617 VIDAR SYSTEMS CORP.
K993598 10/25/1999 MAMMOGRAPHY PRO, MODEL 13017, DIAGNOSTIC PRO W/ MAMMOGRAPHY OPTION, MODEL 13205 VIDAR SYSTEMS CORP.
K993599 10/25/1999 DIAGNOSTIC PRO, MODEL 12772, VXR-16, MODEL 13020, VXR-16 DOSIMETRY PRO, MODEL 13019 VIDAR SYSTEMS CORP.


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