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

FDA 510(k) Number Submission Date Device Name Applicant
K011325 05/01/2001 MEDIFIX URETEROSCOPE MEDIFIX, INC.
K992480 07/26/1999 MEDIFIX SINGLE AND DOUBLE PUNCTURE LAPAROSCOPES MEDIFIX, INC.
K992483 07/26/1999 MEDIFIX INC. MEDIFIX, INC.
K992474 07/26/1999 ARTHROSCOPE / MEDIFIX INC. MEDIFIX, INC.


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