K-number	K782156
Device name	UNITEST CREATINE KINASE
Applicant	Boehringer Mannheim Corp.
Product code	JLB
Device class	Class I
Decision date	Mar 2, 1979
Decision	Substantially Equivalent
Regulation	862.1210

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View the full FDA submission: accessdata.fda.gov

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UNITEST CREATINE KINASE

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