K-number	K180797
Device name	Xcess Guiding Catheter
Applicant	Curatia Medical Co.
Product code	DQY
Device class	Class II
Decision date	Dec 14, 2018
Decision	Substantially Equivalent
Regulation	870.1250

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Source

View the full FDA submission: accessdata.fda.gov

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Xcess Guiding Catheter

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