K-number	K033847
Device name	A1CNOW FOR HOME AND PROFESSIONAL USE
Applicant	Metrika, Inc.
Product code	LCP
Device class	Class II
Decision date	Dec 23, 2003
Decision	Substantially Equivalent
Regulation	864.7470

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View the full FDA submission: accessdata.fda.gov

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A1CNOW FOR HOME AND PROFESSIONAL USE

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