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RELIEF BAND (T.E.N.S. DEVICE)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901704
510(k) Type
Traditional
Applicant
MAVEN LABS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/1991
Days to Decision
586 days

RELIEF BAND (T.E.N.S. DEVICE)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901704
510(k) Type
Traditional
Applicant
MAVEN LABS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/1991
Days to Decision
586 days