K-number	K231820
Device name	SoloSmart Injection Pen Adapter (SoloSmart®)
Applicant	Biocorp Production
Product code	QOG
Device class	Class II
Decision date	Jan 12, 2024
Decision	Substantially Equivalent
Regulation	880.5860

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Source

View the full FDA submission: accessdata.fda.gov

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SoloSmart Injection Pen Adapter (SoloSmart®)

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