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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