K-number	K072141
Device name	S40 CLINICAL ANALYZER, S TEST IP, S TEST UA
Applicant	Alfa Wassermann Diagnostic Technologies, Inc.
Product code	CEO
Device class	Class I
Decision date	Jun 24, 2008
Decision	Substantially Equivalent
Regulation	862.1580

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View the full FDA submission: accessdata.fda.gov

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S40 CLINICAL ANALYZER, S TEST IP, S TEST UA

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