K-number	K841501
Device name	LIFESCOPE 6 OEC-6102
Applicant	Nihon Kohden America, Inc.
Product code	DRT
Device class	Class II
Decision date	Aug 28, 1984
Decision	Substantially Equivalent
Regulation	870.2300

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View the full FDA submission: accessdata.fda.gov

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LIFESCOPE 6 OEC-6102

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