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FDA 510(k)

DUO1 and DUO2

K-Number: K241649 · 2024-07-05

ApplicantZinnovi, Inc.
Decision Date2024-07-05
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DUO1 and DUO2 is a medical device manufactured by Zinnovi, Inc.. It received FDA 510(k) clearance on 2024-07-05 under approval number K241649. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUO1 and DUO2?

DUO1 and DUO2 is a medical device that received FDA 510(k) clearance on 2024-07-05. It is manufactured by Zinnovi, Inc.. The 510(k) number is K241649.

When was DUO1 and DUO2 approved by the FDA?

DUO1 and DUO2 received FDA 510(k) clearance on 2024-07-05, under approval number K241649.

What company makes DUO1 and DUO2?

DUO1 and DUO2 is manufactured by Zinnovi, Inc..

What is the FDA product code for DUO1 and DUO2?

The FDA product code for DUO1 and DUO2 is MUH.

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Official Source

View on FDA Database →

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

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