K-number	K980638
Device name	ADI SYPHILIS RPR LIQUID CONTROLS
Applicant	Ampcor Diagnostics, Inc.
Product code	GMP
Device class	Class II
Decision date	Jul 6, 1998
Decision	Substantially Equivalent
Regulation	866.3820

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View the full FDA submission: accessdata.fda.gov

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ADI SYPHILIS RPR LIQUID CONTROLS

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