K-number	K082704
Device name	BIRTHTRACK (A.K.A. CLM)
Applicant	Barnev, Ltd.
Product code	NPB
Device class	Class II
Decision date	Jan 9, 2009
Decision	Substantially Equivalent
Regulation	884.2800

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View the full FDA submission: accessdata.fda.gov

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BIRTHTRACK (A.K.A. CLM)

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