K-number	K860167
Device name	PRODIGY AND PRODIGY PLUS
Applicant	Cardiodata Corp.
Product code	DSI
Device class	Class II
Decision date	Mar 31, 1986
Decision	Substantially Equivalent
Regulation	870.1025

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Source

View the full FDA submission: accessdata.fda.gov

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PRODIGY AND PRODIGY PLUS

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