K-number	K200321
Device name	Novaerus NV1050
Applicant	Novaerus Us, Inc.
Product code	FRF
Device class	Class II
Decision date	Dec 28, 2020
Decision	Substantially Equivalent
Regulation	880.5045

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Source

View the full FDA submission: accessdata.fda.gov

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Novaerus NV1050

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