K-number	K013912
Device name	CREATINE KINASE (CK-NAC)
Applicant	Jas Diagnostics, Inc.
Product code	CGS
Device class	Class II
Decision date	Jan 18, 2002
Decision	Substantially Equivalent
Regulation	862.1215

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View the full FDA submission: accessdata.fda.gov

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CREATINE KINASE (CK-NAC)

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