K-number	K882032
Device name	MODEL 90DX MULTITEST METER
Applicant	Mesa Medical, Inc.
Product code	FLB
Device class	Class II
Decision date	Aug 11, 1988
Decision	Substantially Equivalent
Regulation	876.5820

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View the full FDA submission: accessdata.fda.gov

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MODEL 90DX MULTITEST METER

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