K-number	K925210
Device name	90DX MULTITEST METER, MODIFICATION
Applicant	Mesa Medical, Inc.
Product code	FLB
Device class	Class II
Decision date	Jan 25, 1994
Decision	Substantially Equivalent
Regulation	876.5820

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View the full FDA submission: accessdata.fda.gov

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90DX MULTITEST METER, MODIFICATION

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