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ELECTROPULSE

Page Type
Cleared 510(K)
510(k) Number
K051128
510(k) Type
Traditional
Applicant
PAIN RELIEF TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/2006
Days to Decision
311 days
Submission Type
Statement

ELECTROPULSE

Page Type
Cleared 510(K)
510(k) Number
K051128
510(k) Type
Traditional
Applicant
PAIN RELIEF TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/2006
Days to Decision
311 days
Submission Type
Statement