K-number	K231342
Device name	Insufflator (OPTO-IFL1000)
Applicant	Guangdong Optomedic Technologies, Inc.
Product code	HIF
Device class	Class II
Decision date	Sep 20, 2023
Decision	Substantially Equivalent
Regulation	884.1730

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View the full FDA submission: accessdata.fda.gov

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Insufflator (OPTO-IFL1000)

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