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FDA 510(k)

Revital Cady

K-Number: K231519 · 2023-11-06

ApplicantRevital Healthcare (Epz) Limited
Decision Date2023-11-06
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Revital Cady is a medical device manufactured by Revital Healthcare (Epz) Limited. It received FDA 510(k) clearance on 2023-11-06 under approval number K231519. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Revital Cady?

Revital Cady is a medical device that received FDA 510(k) clearance on 2023-11-06. It is manufactured by Revital Healthcare (Epz) Limited. The 510(k) number is K231519.

When was Revital Cady approved by the FDA?

Revital Cady received FDA 510(k) clearance on 2023-11-06, under approval number K231519.

What company makes Revital Cady?

Revital Cady is manufactured by Revital Healthcare (Epz) Limited.

What is the FDA product code for Revital Cady?

The FDA product code for Revital Cady is FMF.

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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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