K-number	K922170
Device name	AMERLITE PROLACTIN-30 ASSAY
Applicant	Eastman Kodak Company
Product code	CFT
Device class	Class I
Decision date	Sep 2, 1992
Decision	Substantially Equivalent
Regulation	862.1625

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View the full FDA submission: accessdata.fda.gov

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AMERLITE PROLACTIN-30 ASSAY

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