K-number	K922351
Device name	QUANTA LITE(TM) IGA ACA
Applicant	Inova Diagnostics, Inc.
Product code	MID
Device class	Class II
Decision date	Sep 29, 1992
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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QUANTA LITE(TM) IGA ACA

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