FDA 510(k)

Revitive Medic Plus, Revitive Advanced 2

K-Number: K192887 · 2020-05-04

Decision Date2020-05-04

Product CodeNGX

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

Revitive Medic Plus, Revitive Advanced 2 is a medical device manufactured by Actegy , Ltd.. It received FDA 510(k) clearance on 2020-05-04 under approval number K192887. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Revitive Medic Plus, Revitive Advanced 2?

Revitive Medic Plus, Revitive Advanced 2 is a medical device that received FDA 510(k) clearance on 2020-05-04. It is manufactured by Actegy , Ltd.. The 510(k) number is K192887.

When was Revitive Medic Plus, Revitive Advanced 2 approved by the FDA?

Revitive Medic Plus, Revitive Advanced 2 received FDA 510(k) clearance on 2020-05-04, under approval number K192887.

What company makes Revitive Medic Plus, Revitive Advanced 2?

Revitive Medic Plus, Revitive Advanced 2 is manufactured by Actegy , Ltd..

What is the FDA product code for Revitive Medic Plus, Revitive Advanced 2?

The FDA product code for Revitive Medic Plus, Revitive Advanced 2 is NGX.

Other Devices by Actegy , Ltd.

K152480Revitive Medic; Revitive MV; Revitive LV K190924Revitive Medic Plus, Revitive Advanced 2 K210825Revitive Medic Coach (Model Number 5575AQ)

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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.