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FDA 510(k)

Virtus Metabolic Monitor

K-Number: K222982 · 2023-06-23

ApplicantVirtus Technology Aps
Decision Date2023-06-23
Product CodeBTY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Virtus Metabolic Monitor is a medical device manufactured by Virtus Technology Aps. It received FDA 510(k) clearance on 2023-06-23 under approval number K222982. The device is classified under product code BTY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Virtus Metabolic Monitor?

Virtus Metabolic Monitor is a medical device that received FDA 510(k) clearance on 2023-06-23. It is manufactured by Virtus Technology Aps. The 510(k) number is K222982.

When was Virtus Metabolic Monitor approved by the FDA?

Virtus Metabolic Monitor received FDA 510(k) clearance on 2023-06-23, under approval number K222982.

What company makes Virtus Metabolic Monitor?

Virtus Metabolic Monitor is manufactured by Virtus Technology Aps.

What is the FDA product code for Virtus Metabolic Monitor?

The FDA product code for Virtus Metabolic Monitor is BTY.

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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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