K-number	K852224
Device name	LEE-BEAD TSH(EIA)
Applicant	Lecco Diagnostics, Inc.
Product code	JLW
Device class	Class II
Decision date	Jul 9, 1985
Decision	Substantially Equivalent
Regulation	862.1690

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View the full FDA submission: accessdata.fda.gov

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LEE-BEAD TSH(EIA)

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