K-number	K922742
Device name	HPM 40 HEART PACEMAKER MONITOR
Applicant	Biotronik, GmbH & Co.
Product code	KRE
Device class	Class II
Decision date	Mar 18, 1993
Decision	Substantially Equivalent
Regulation	870.3640

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View the full FDA submission: accessdata.fda.gov

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HPM 40 HEART PACEMAKER MONITOR

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