K-number	K863587
Device name	CREATINE PHOSPHOKINASE(CK) PROCEDURE
Applicant	Data Medical Associates, Inc.
Product code	CGS
Device class	Class II
Decision date	Oct 3, 1986
Decision	Substantially Equivalent
Regulation	862.1215

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View the full FDA submission: accessdata.fda.gov

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CREATINE PHOSPHOKINASE(CK) PROCEDURE

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