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AUDITORY STIMULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K813557
510(k) Type
Traditional
Applicant
WESTERN ADVANCED TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1982
Days to Decision
28 days

AUDITORY STIMULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K813557
510(k) Type
Traditional
Applicant
WESTERN ADVANCED TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1982
Days to Decision
28 days