K-number	K022280
Device name	STOCKERT CORONARY PERFUSION CANNULAE
Applicant	Stockert Instrumente GmbH
Product code	DWF
Device class	Class II
Decision date	Oct 11, 2002
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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STOCKERT CORONARY PERFUSION CANNULAE

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