FDA 510(k)

NeutrArt

K-Number: K221481 · 2022-09-23

Decision Date2022-09-23

Product CodeFPA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

NeutrArt is a medical device manufactured by Asset Medikal Tasarim As.. It received FDA 510(k) clearance on 2022-09-23 under approval number K221481. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NeutrArt?

NeutrArt is a medical device that received FDA 510(k) clearance on 2022-09-23. It is manufactured by Asset Medikal Tasarim As.. The 510(k) number is K221481.

When was NeutrArt approved by the FDA?

NeutrArt received FDA 510(k) clearance on 2022-09-23, under approval number K221481.

What company makes NeutrArt?

NeutrArt is manufactured by Asset Medikal Tasarim As..

What is the FDA product code for NeutrArt?

The FDA product code for NeutrArt is FPA.

Other Devices by Asset Medikal Tasarim As.

K190806Flowart K201872NeutrArt K221473Flowart

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.