K-number	K831354
Device name	EMIT QST LIDOCAINE ASSAY
Applicant	Syva Co.
Product code	KLR
Device class	Class II
Decision date	May 27, 1983
Decision	Substantially Equivalent
Regulation	862.3555

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View the full FDA submission: accessdata.fda.gov

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EMIT QST LIDOCAINE ASSAY

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