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FDA 510(k)

Meron Plus QM

K-Number: K180386 · 2018-05-08

ApplicantVoco GmbH
Decision Date2018-05-08
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Meron Plus QM is a medical device manufactured by Voco GmbH. It received FDA 510(k) clearance on 2018-05-08 under approval number K180386. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Meron Plus QM?

Meron Plus QM is a medical device that received FDA 510(k) clearance on 2018-05-08. It is manufactured by Voco GmbH. The 510(k) number is K180386.

When was Meron Plus QM approved by the FDA?

Meron Plus QM received FDA 510(k) clearance on 2018-05-08, under approval number K180386.

What company makes Meron Plus QM?

Meron Plus QM is manufactured by Voco GmbH.

What is the FDA product code for Meron Plus QM?

The FDA product code for Meron Plus QM is EMA.

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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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