K-number	K962551
Device name	CARDIOSERV S
Applicant	Marquette Electronics, Inc.
Product code	LDD
Device class	Class II
Decision date	Nov 19, 1996
Decision	Substantially Equivalent - Subject to Tracking Reg.
Regulation	870.5300

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View the full FDA submission: accessdata.fda.gov

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CARDIOSERV S

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