K-number	K772109
Device name	IN VITRO HUMAN TSH RIA TEST
Applicant	Clinical Assays, Inc.
Product code	JLW
Device class	Class II
Decision date	Dec 6, 1977
Decision	Substantially Equivalent
Regulation	862.1690

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View the full FDA submission: accessdata.fda.gov

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IN VITRO HUMAN TSH RIA TEST

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