REVITIVE IX— 510(k) K123354

Substantially Equivalent

Actegy , Ltd.

FDA 510(k) clearance K123354 for REVITIVE IX, Substantially Equivalent on 2013-06-28. Applicant: Actegy , Ltd.. Device class: 2.

Clearance details

Applicant: Actegy , Ltd.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2012-10-31
Decision date: 2013-06-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.