K-number	K202120
Device name	P300 Attachment
Applicant	Nakanishi, Inc.
Product code	HBE
Device class	Class II
Decision date	Oct 22, 2021
Decision	Substantially Equivalent
Regulation	882.4310

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Source

View the full FDA submission: accessdata.fda.gov

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P300 Attachment

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