K-number	K971304
Device name	QUANTA LITE REBELLA IGG
Applicant	Inova Diagnostics, Inc.
Product code	LFX
Device class	Class II
Decision date	Jan 2, 1998
Decision	Substantially Equivalent
Regulation	866.3510

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View the full FDA submission: accessdata.fda.gov

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QUANTA LITE REBELLA IGG

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