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AD-TECH SUBDURAL ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K970587
510(k) Type
Traditional
Applicant
AD-TECH MEDICAL INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1997
Days to Decision
80 days
Submission Type
Statement

AD-TECH SUBDURAL ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K970587
510(k) Type
Traditional
Applicant
AD-TECH MEDICAL INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1997
Days to Decision
80 days
Submission Type
Statement