K-number	K821090
Device name	CARDI-O-LIFE MODEL 8823
Applicant	Amertek
Product code	DPS
Device class	Class II
Decision date	Jul 8, 1982
Decision	Substantially Equivalent
Regulation	870.2340

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View the full FDA submission: accessdata.fda.gov

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CARDI-O-LIFE MODEL 8823

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