K-number	K896184
Device name	KALOS 05 PULSE GENERATOR
Applicant	Biotronik Cardiac Pacemakers
Product code	DXY
Device class	Class III
Decision date	Jan 18, 1990
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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KALOS 05 PULSE GENERATOR

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