K-number	K171491
Device name	R2P Destination Slender Guiding Sheath
Applicant	Terumo Medical Corporation
Product code	DYB
Device class	Class II
Decision date	Oct 5, 2017
Decision	Substantially Equivalent
Regulation	870.1340

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Source

View the full FDA submission: accessdata.fda.gov

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R2P Destination Slender Guiding Sheath

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