K-number	K810548
Device name	CARDIOPULMINARY BYPASS CATHETER CANNULA
Applicant	Dlp, Inc.
Product code	DWF
Device class	Class II
Decision date	Mar 17, 1981
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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CARDIOPULMINARY BYPASS CATHETER CANNULA

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