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WYLER SPHENOIDAL ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861031
510(k) Type
Traditional
Applicant
AD-TECH MEDICAL INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/1986
Days to Decision
160 days

WYLER SPHENOIDAL ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861031
510(k) Type
Traditional
Applicant
AD-TECH MEDICAL INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/1986
Days to Decision
160 days