K-number	K223785
Device name	N9+
Applicant	Nonagon , Ltd.
Product code	DQD
Device class	Class II
Decision date	Apr 14, 2023
Decision	Substantially Equivalent
Regulation	870.1875

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Source

View the full FDA submission: accessdata.fda.gov

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N9+

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