K-number	K802058
Device name	MAPPING PROBE MODEL #6540
Applicant	Cardiac Pacemakers, Inc.
Product code	DRF
Device class	Class II
Decision date	Nov 19, 1980
Decision	Substantially Equivalent
Regulation	870.1220

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View the full FDA submission: accessdata.fda.gov

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MAPPING PROBE MODEL #6540

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