K-number	K880477
Device name	RPR TEST FOR SYPHILIS IN SERUM OR PLASMA
Applicant	Ampcor, Inc.
Product code	GMQ
Device class	Class II
Decision date	Mar 30, 1988
Decision	Substantially Equivalent
Regulation	866.3820

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View the full FDA submission: accessdata.fda.gov

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RPR TEST FOR SYPHILIS IN SERUM OR PLASMA

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