K-number	K781738
Device name	PACEMAKER, MODEL 229-01
Applicant	Intermedics, Inc.
Product code	DXY
Device class	Class III
Decision date	Dec 7, 1978
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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PACEMAKER, MODEL 229-01

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