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FDA 510(k) Applications Submitted by KARA KANORR
FDA 510(k) Number
Submission Date
Device Name
Applicant
K160217
01/29/2016
uVue HSG/SHG Catheter
COOK INCORPORATED
K160891
03/31/2016
Ultrathane Endoureterotomy Stent Set
Cook Incorporated
K162109
07/29/2016
Kwart Retro-Inject Ureteral Stent
COOK INCORPORATED
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