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FDA 510(k) Applications Submitted by JAMES W KRONBERG
FDA 510(k) Number
Submission Date
Device Name
Applicant
K060669
03/14/2006
MEDRELIEF ST SERIES, MODELS RT-50, ST-100, ST 150, ST-200, ST-300
HEALTHONICS, INC.
K030998
03/31/2003
MEDRELIEF SE SERIES, MODELS SE-50, SE-100, SE-200, SE-300
HEALTHONICS, INC.
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