K-number	K203792
Device name	Insupen Pen needle, Insupen ORIGINAL Pen Needle, Insupen ADVANCED pen needle
Applicant	Pikdare Spa
Product code	FMI
Device class	Class II
Decision date	Jan 20, 2023
Decision	Substantially Equivalent
Regulation	880.5570

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Source

View the full FDA submission: accessdata.fda.gov

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Insupen Pen needle, Insupen ORIGINAL Pen Needle, Insupen ADVANCED pen needle

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