K-number	K020241
Device name	QACA IGG/IGM ELISA KIT
Applicant	Cheshire Diagnostics , Ltd.
Product code	MID
Device class	Class II
Decision date	Mar 13, 2002
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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QACA IGG/IGM ELISA KIT

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