FDA 510(k) Applications Submitted by FREERIDER USA, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K971387 04/14/1997 FREERIDER, MODEL FR510-F FREERIDER USA, INC.
K971388 04/14/1997 FREERIDER, MODEL FR168-4 FREERIDER USA, INC.


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