FDA 510(k) Applications Submitted by STEVEN ARICK

FDA 510(k) Number Submission Date Device Name Applicant
K030999 03/31/2003 EPTFE VASCULAR PROSTHESIS; SEALPTFE VASCUTEK LTD.
K040829 03/31/2004 GELWEAVE ANTE-FLO WITH COLLAR AND GELWEAVE 4 BRANCH PLEXUS WITH COLLAR VASCUTEK LTD.
K041528 06/08/2004 MODIFICATION TO EPTFE GRAFT VASCUTEK LTD.
K034010 12/24/2003 GELSOFT PLUS ERS VASCUTEK LTD.
K043552 12/27/2004 VASCUTEK PTFE SUPPORTED EPTFE VASCULAR PROSTHESES VASCUTEK LTD.


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