K-number	K812813
Device name	INTERMEDICS PROGRAMMER, MODEL 522-03
Applicant	Intermedics, Inc.
Product code	KRG
Device class	Class III
Decision date	Oct 27, 1981
Decision	Substantially Equivalent
Regulation	870.3700

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View the full FDA submission: accessdata.fda.gov

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INTERMEDICS PROGRAMMER, MODEL 522-03

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