K-number	K223347
Device name	UltraSight AI Guidance
Applicant	Ultrasight, Inc.
Product code	QJU
Device class	Class II
Decision date	Jul 24, 2023
Decision	Substantially Equivalent
Regulation	892.2100

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Source

View the full FDA submission: accessdata.fda.gov

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UltraSight AI Guidance

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