LOW BACK PAIN RELIEF SYSTEM /MODELS GM310PP,GM320PP,GM321PP, AND GM330PP— 510(k) K060222
Substantially EquivalentGemore Technology Co, Ltd.
FDA 510(k) clearance K060222 for LOW BACK PAIN RELIEF SYSTEM /MODELS GM310PP,GM320PP,GM321PP, AND GM330PP, Substantially Equivalent on 2006-04-28. Applicant: Gemore Technology Co, Ltd.. Device class: 2.
Clearance details
- Applicant
- Gemore Technology Co, Ltd.
- 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
- Tan Shui, New Taipei City, TW
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