K-number	K062092
Device name	PREVU POINT OF CARE SKIN STEROL TEST
Applicant	Premd, Inc.
Product code	LBS
Device class	Class I
Decision date	Sep 15, 2006
Decision	Unknown
Regulation	862.1475

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Source

View the full FDA submission: accessdata.fda.gov

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PREVU POINT OF CARE SKIN STEROL TEST

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