Last synced on 25 January 2026 at 3:41 am

LOW BACK PAIN RELIEF SYSTEM /MODELS GM310PP,GM320PP,GM321PP, AND GM330PP

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060222
510(k) Type
Traditional
Applicant
Gemore Technology Co, Ltd.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
4/28/2006
Days to Decision
88 days
Submission Type
Summary

LOW BACK PAIN RELIEF SYSTEM /MODELS GM310PP,GM320PP,GM321PP, AND GM330PP

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060222
510(k) Type
Traditional
Applicant
Gemore Technology Co, Ltd.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
4/28/2006
Days to Decision
88 days
Submission Type
Summary