MYOTouch Muscle Stimulator— 510(k) K233098

Substantially Equivalent

Sunmed, LLC

FDA 510(k) clearance K233098 for MYOTouch Muscle Stimulator, Substantially Equivalent on 2024-08-02. Applicant: Sunmed, LLC.

Clearance details

Applicant: Sunmed, LLC
Product code: Code IPF
Advisory panel: Physical Medicine
Date received: 2023-09-26
Decision date: 2024-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grand Rapids, MI, US

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