K-number	K821100
Device name	MERITECASTREP (TM)
Applicant	Meridian Diagnostics, Inc.
Product code	GTZ
Device class	Class I
Decision date	May 13, 1982
Decision	Substantially Equivalent
Regulation	866.3740

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View the full FDA submission: accessdata.fda.gov

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MERITECASTREP (TM)

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