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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