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ELECTROPULSE - LOW BACK PAIN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062532
510(k) Type
Traditional
Applicant
PAIN RELIEF TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/2007
Days to Decision
165 days
Submission Type
Statement

ELECTROPULSE - LOW BACK PAIN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062532
510(k) Type
Traditional
Applicant
PAIN RELIEF TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/2007
Days to Decision
165 days
Submission Type
Statement