Erchonia GVL— 510(k) K221987

Substantially Equivalent

Erchonia Corporation

FDA 510(k) clearance K221987 for Erchonia GVL, Substantially Equivalent on 2022-09-01. Applicant: Erchonia Corporation.

Clearance details

Applicant: Erchonia Corporation
Product code: Code NHN
Advisory panel: Physical Medicine
Date received: 2022-07-06
Decision date: 2022-09-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Melbourne, FL, US

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