K-number	K050338
Device name	MODIFICATION TO: INSTAREAD LITHIUM SYSTEM
Applicant	Akers Biosciences, Inc.
Product code	JIH
Device class	Class II
Decision date	Mar 4, 2005
Decision	Substantially Equivalent
Regulation	862.3560

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO: INSTAREAD LITHIUM SYSTEM

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