Erchonia PL Touch— 510(k) K153052

Substantially Equivalent

Erchonia Corporation

FDA 510(k) clearance K153052 for Erchonia PL Touch, Substantially Equivalent on 2016-01-04. Applicant: Erchonia Corporation. Device class: 2.

Clearance details

Applicant: Erchonia Corporation
Product code: Code NHN
Device class: Class 2
Regulation: 21 CFR 890.5500
Advisory panel: Physical Medicine
Date received: 2015-10-20
Decision date: 2016-01-04
Decision: Substantially Equivalent
Clearance type: Special
Location: Mckinney, TX, 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.