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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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