K-number	K842368
Device name	SICKLE CELL REAGENT SET
Applicant	Livonia Diagnostics, Inc.
Product code	GHM
Device class	Class II
Decision date	Jul 20, 1984
Decision	Substantially Equivalent
Regulation	864.7825

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View the full FDA submission: accessdata.fda.gov

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SICKLE CELL REAGENT SET

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