K-number	K942159
Device name	NOVOPEN 1.5
Applicant	Novo Nordisk Pharmaceuticals, Inc.
Product code	FMF
Device class	Class II
Decision date	Apr 26, 1995
Decision	Substantially Equivalent
Regulation	880.5860

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View the full FDA submission: accessdata.fda.gov

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NOVOPEN 1.5

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