Last synced on 24 May 2024 at 11:04 pm

TENS DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812138
510(k) Type
Traditional
Applicant
WESTERN ADVANCED TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/1981
Days to Decision
23 days

TENS DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812138
510(k) Type
Traditional
Applicant
WESTERN ADVANCED TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/1981
Days to Decision
23 days