K-number	K820230
Device name	PACEMAKER PROGRAMMER 2030
Applicant	Cardiac Pacemakers, Inc.
Product code	KRG
Device class	Class III
Decision date	Mar 15, 1982
Decision	Substantially Equivalent
Regulation	870.3700

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View the full FDA submission: accessdata.fda.gov

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PACEMAKER PROGRAMMER 2030

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