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FDA 510(k) Applications for Medical Device Product Code "DQT"
(Occluder, Catheter Tip)
FDA 510(k) Number
Applicant
Device Name
Decision Date
K983927
ARTERIAL VASCULAR ENGINEERING, INC.
GT1 FLOPPY, GT1 HI-PER FLEX, GT1 LIGHT SUPPORT
03/11/1999
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