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FDA 510(k)

IMICRYL Composite, Composite Flow Materials

K-Number: K220077 · 2022-08-09

Decision Date2022-08-09
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMICRYL Composite, Composite Flow Materials is a medical device manufactured by Imicryl Dis Malzemeleri Sanayi VE Ticaret AS. It received FDA 510(k) clearance on 2022-08-09 under approval number K220077. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMICRYL Composite, Composite Flow Materials?

IMICRYL Composite, Composite Flow Materials is a medical device that received FDA 510(k) clearance on 2022-08-09. It is manufactured by Imicryl Dis Malzemeleri Sanayi VE Ticaret AS. The 510(k) number is K220077.

When was IMICRYL Composite, Composite Flow Materials approved by the FDA?

IMICRYL Composite, Composite Flow Materials received FDA 510(k) clearance on 2022-08-09, under approval number K220077.

What company makes IMICRYL Composite, Composite Flow Materials?

IMICRYL Composite, Composite Flow Materials is manufactured by Imicryl Dis Malzemeleri Sanayi VE Ticaret AS.

What is the FDA product code for IMICRYL Composite, Composite Flow Materials?

The FDA product code for IMICRYL Composite, Composite Flow Materials is EBF.

Related Clinical Trials

Other Devices by Imicryl Dis Malzemeleri Sanayi VE Ticaret AS

Related Devices (Code: EBF)

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.