FDA 510(k)

Flowart

K-Number: K221473 · 2022-09-26

Decision Date2022-09-26

Product CodeFPA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

Flowart is a medical device manufactured by Asset Medikal Tasarim As.. It received FDA 510(k) clearance on 2022-09-26 under approval number K221473. 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 Flowart?

Flowart is a medical device that received FDA 510(k) clearance on 2022-09-26. It is manufactured by Asset Medikal Tasarim As.. The 510(k) number is K221473.

When was Flowart approved by the FDA?

Flowart received FDA 510(k) clearance on 2022-09-26, under approval number K221473.

What company makes Flowart?

Flowart is manufactured by Asset Medikal Tasarim As..

What is the FDA product code for Flowart?

The FDA product code for Flowart is FPA.

Other Devices by Asset Medikal Tasarim As.

K190806Flowart K201872NeutrArt K221481NeutrArt

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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.