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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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