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FDA 510(k) Applications Submitted by SCOTT MOELLER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K031718
06/03/2003
LIFEVALVE CENTRAL VENOUS CATHTER
HORIZON MEDICAL PRODUCTS, INC.
K032557
08/19/2003
TRIUMPH VTX WITH LIFEVALVE CATHETER
HORIZON MEDICAL PRODUCTS, INC.
K022905
09/03/2002
LIFEJET F16 HEMODIALYSIS/APHERESIS CHRONIC CATHETER
HORIZON MEDICAL PRODUCTS, INC.
K032754
09/05/2003
VORTEX MP
HORIZON MEDICAL PRODUCTS, INC.
K033473
11/03/2003
MODIFICATION TO VORTEX MP VASCULAR ACCESS PORT
HORIZON MEDICAL PRODUCTS, INC.
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