K-number	K221481
Device name	NeutrArt
Applicant	Asset Medikal Tasarim As.
Product code	FPA
Device class	Class II
Decision date	Sep 23, 2022
Decision	Substantially Equivalent
Regulation	880.5440

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Source

View the full FDA submission: accessdata.fda.gov

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NeutrArt

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