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FDA 510(k) Applications Submitted by DAN ANDERSON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K954922
10/26/1995
REXTON'S HORIZION FAMILY OF MULTIPLE SITUATION, SINGLE CHANNEL PROGRAMMBALE INSTRUMENTS
REXTON, INC.
K960295
01/22/1996
LONG LIFE RX-12
REXTON, INC.
K964451
11/06/1996
PICCOLO K-AMP VC+, PICCOLO P-A1, PICCOLO P-AO AND PICCOLO ATC
REXTON, INC.
K970537
02/12/1997
REXTON MODEL 48 AND 49PP
REXTON, INC.
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