K-number	K222292
Device name	F&P myAirvo 3
Applicant	Fisher & Paykel Healthcare
Product code	BTT
Device class	Class II
Decision date	May 8, 2024
Decision	Substantially Equivalent
Regulation	868.5450

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Source

View the full FDA submission: accessdata.fda.gov

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F&P myAirvo 3

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