TMJ Relax— 510(k) K202523

Name: FDA 510(k) clearance K202523
Creator: U.S. Food and Drug Administration
Published: 2021-06-24

Substantially Equivalent

Moonwalker Innovations, Inc.

FDA 510(k) clearance K202523 for TMJ Relax, Substantially Equivalent on 2021-06-24. Applicant: Moonwalker Innovations, Inc.. Device class: Unclassified.

Clearance details

Applicant: Moonwalker Innovations, Inc.
Product code: Code OCO
Device class: Unclassified
Advisory panel: Unknown
Date received: 2020-09-01
Decision date: 2021-06-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Medford, MA, US

Download summary PDF View on FDA.gov ↗

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