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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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