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FDA 510(k)

Colibrí

K-Number: K223245 · 2023-03-20

Decision Date2023-03-20
Product CodeQQV
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

Colibrí is a medical device manufactured by Copan Wasp Srl. It received FDA 510(k) clearance on 2023-03-20 under approval number K223245. The device is classified under product code QQV. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Colibrí?

Colibrí is a medical device that received FDA 510(k) clearance on 2023-03-20. It is manufactured by Copan Wasp Srl. The 510(k) number is K223245.

When was Colibrí approved by the FDA?

Colibrí received FDA 510(k) clearance on 2023-03-20, under approval number K223245.

What company makes Colibrí?

Colibrí is manufactured by Copan Wasp Srl.

What is the FDA product code for Colibrí?

The FDA product code for Colibrí is QQV.

Other Devices by Copan Wasp Srl

Related Devices (Code: QQV)

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.