K-number	K162214
Device name	Protek Solo 24 Fr Venous Cannula Set
Applicant	Cardiacassist, Inc.
Product code	DWF
Device class	Class II
Decision date	Nov 30, 2016
Decision	Substantially Equivalent
Regulation	870.4210

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Source

View the full FDA submission: accessdata.fda.gov

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Protek Solo 24 Fr Venous Cannula Set

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