CP Relief Wand-OTC— 510(k) K162630
Substantially EquivalentMid-America Medical Innovations, LLC
FDA 510(k) clearance K162630 for CP Relief Wand-OTC, Substantially Equivalent on 2016-12-20. Applicant: Mid-America Medical Innovations, LLC. Device class: 2.
Clearance details
- Applicant
- Mid-America Medical Innovations, LLC
- Product code
- Code NUH
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Jefferson City, MO, US
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