K-number	K854487
Device name	VENOUS RETURN CANNULA W/CUFF 91039
Applicant	Dlp, Inc.
Product code	DWF
Device class	Class II
Decision date	Feb 10, 1986
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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VENOUS RETURN CANNULA W/CUFF 91039

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