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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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