Revitive Medic; Revitive MV; Revitive LV— 510(k) K152480

Name: FDA 510(k) clearance K152480
Creator: U.S. Food and Drug Administration
Published: 2016-03-31

Substantially Equivalent

Actegy , Ltd.

FDA 510(k) clearance K152480 for Revitive Medic; Revitive MV; Revitive LV, Substantially Equivalent on 2016-03-31. Applicant: Actegy , Ltd.. Device class: 2.

Clearance details

Applicant: Actegy , Ltd.
Product code: Code NGX
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2015-08-31
Decision date: 2016-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bracknell, GB

Download summary PDF View on FDA.gov ↗

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