FDA 510(k) Applications Submitted by THERATRONICS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K954679 10/10/1995 THERAPLAN PLUS THERATRONICS, INC.
K970236 01/21/1997 THERAPLAN PLUS VERSION 1.2 THERATRONICS, INC.
K983917 11/04/1998 THERATRON ELITE THERATRONICS, INC.
K964606 11/18/1996 THERATRON 780E THERATRONICS, INC.
K964607 11/18/1996 THERATON 1000E THERATRONICS, INC.


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