K-number	K861945
Device name	LEE-BEAD PROLACTIN (EIA)
Applicant	Leeco Diagnostics, Inc.
Product code	CFT
Device class	Class I
Decision date	Jun 13, 1986
Decision	Substantially Equivalent
Regulation	862.1625

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View the full FDA submission: accessdata.fda.gov

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LEE-BEAD PROLACTIN (EIA)

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