FDA 510(k) Applications Submitted by ARTERIAL VASCULAR ENGINEERING, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K983927 11/05/1998 GT1 FLOPPY, GT1 HI-PER FLEX, GT1 LIGHT SUPPORT ARTERIAL VASCULAR ENGINEERING, INC.
K984627 12/30/1998 AVE 4F SITESEER CARDIOVASCULAR ANGIOGRAPHIC CATHETER ARTERIAL VASCULAR ENGINEERING, INC.
K971295 04/07/1997 AVE BRIDGE STENT SYSTEM ARTERIAL VASCULAR ENGINEERING, INC.


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