K-number	K050546
Device name	ACON +/- MIDSTREAM PREGNANCY TEST
Applicant	ACON Laboratories, Inc.
Product code	LCX
Device class	Class II
Decision date	May 20, 2005
Decision	Substantially Equivalent
Regulation	862.1155

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View the full FDA submission: accessdata.fda.gov

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ACON +/- MIDSTREAM PREGNANCY TEST

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