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FDA 510(k) Applications Submitted by JACK SPEER AND ASSOC., INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K040065
01/13/2004
JSA'S REPROCESSED COMPRESSION SLEEVE DEVICES
JACK SPEER AND ASSOC., INC.
K031722
06/03/2003
JSA REPROCESSED COMPRESSION SLEEVE DEVICES
JACK SPEER AND ASSOC., INC.
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