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FDA 510(k) Applications Submitted by HIMANSHU PATEL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K101647
06/11/2010
WILDCAT 5F GUIDEWIRE SUPPORT CATHETER, MODE W500
AVINGER, INC.
K102022
07/19/2010
WILDCAT 6F GUIDEWIRE SUPPORT CATHETER MODEL W400L AND W400S
AVINGER, INC.
K083313
11/10/2008
WILDCAT 7F GUIDEWIRE SUPPORT CATHETER
AVINGER, INC.
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