K-number	K922109
Device name	KING DIAGNOSTICS ALT (GPT) REAGENT
Applicant	King Diagnostics, Inc.
Product code	CKA
Device class	Class I
Decision date	Jun 4, 1992
Decision	Substantially Equivalent
Regulation	862.1030

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View the full FDA submission: accessdata.fda.gov

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KING DIAGNOSTICS ALT (GPT) REAGENT

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