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RELIEFBAND TENS UNIT (MODIFICATION)

Page Type
Cleared 510(K)
510(k) Number
K961050
510(k) Type
Traditional
Applicant
MAVEN LABS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1997
Days to Decision
540 days
Submission Type
Statement

RELIEFBAND TENS UNIT (MODIFICATION)

Page Type
Cleared 510(K)
510(k) Number
K961050
510(k) Type
Traditional
Applicant
MAVEN LABS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1997
Days to Decision
540 days
Submission Type
Statement