K-number	K952646
Device name	IL TEST CK-MB
Applicant	Instrumentation Laboratory CO
Product code	CGS
Device class	Class II
Decision date	Aug 4, 1995
Decision	Substantially Equivalent
Regulation	862.1215

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View the full FDA submission: accessdata.fda.gov

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IL TEST CK-MB

Everything you need for a 510(k) submission. Nothing you don't.