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

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.
K003507 11/13/2000 MEDRELIEF HEALTHONICS, INC.


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