K-number	K872839
Device name	ANTINUCLEAR ANTIBODY TEST
Applicant	Cappel Diagnostics, Inc.
Product code	LJM
Device class	Class II
Decision date	Oct 20, 1987
Decision	Substantially Equivalent
Regulation	866.5100

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View the full FDA submission: accessdata.fda.gov

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ANTINUCLEAR ANTIBODY TEST

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