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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 the device name listed in this FDA 510(k) record. The listed applicant is Revital Healthcare (Epz) Limited. It received FDA 510(k) clearance on 2023-11-06 under 510(k) 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. The listed applicant is Revital Healthcare (Epz) Limited. The 510(k) number is K231519.

When did Revital Cady receive FDA 510(k) clearance?

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

Who is the listed applicant for Revital Cady?

The FDA 510(k) record lists Revital Healthcare (Epz) Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Revital Cady?

The FDA product code for Revital Cady is FMF.

Related Devices (Code: FMF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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