MYOTouch Muscle Stimulator— 510(k) K233098
Substantially EquivalentSunmed, LLC
FDA 510(k) clearance K233098 for MYOTouch Muscle Stimulator, Substantially Equivalent on 2024-08-02. Applicant: Sunmed, LLC. Device class: 2.
Clearance details
- Applicant
- Sunmed, LLC
- Product code
- Code IPF
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Grand Rapids, MI, US
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