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WYLER SUBDURAL STRIP ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K850342
510(k) Type
Traditional
Applicant
AD-TECH MEDICAL INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/30/1985
Days to Decision
183 days

WYLER SUBDURAL STRIP ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K850342
510(k) Type
Traditional
Applicant
AD-TECH MEDICAL INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/30/1985
Days to Decision
183 days