K-number	K901135
Device name	ENZYMUN TEST(R) INSULIN
Applicant	Boehringer Mannheim Corp.
Product code	CFP
Device class	Class I
Decision date	Apr 3, 1990
Decision	Substantially Equivalent
Regulation	862.1405

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View the full FDA submission: accessdata.fda.gov

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ENZYMUN TEST(R) INSULIN

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