K-number	K811217
Device name	PACEMAKER PROGRAMMER #2010
Applicant	Cardiac Pacemakers, Inc.
Product code	KRG
Device class	Class III
Decision date	Jul 20, 1981
Decision	Substantially Equivalent
Regulation	870.3700

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View the full FDA submission: accessdata.fda.gov

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PACEMAKER PROGRAMMER #2010

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