K-number	K860538
Device name	RIGHT-DAY URINARY LH (EIA)
Applicant	Leeco Diagnostics, Inc.
Product code	CEP
Device class	Class I
Decision date	Jul 29, 1986
Decision	Substantially Equivalent
Regulation	862.1485

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View the full FDA submission: accessdata.fda.gov

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RIGHT-DAY URINARY LH (EIA)

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