K-number	K792695
Device name	ANTI-GLOBULIN CONTROL
Applicant	Meridian Diagnostics, Inc.
Product code	DHR
Device class	Class II
Decision date	Jan 24, 1980
Decision	Substantially Equivalent
Regulation	866.5775

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View the full FDA submission: accessdata.fda.gov

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ANTI-GLOBULIN CONTROL

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