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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