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DUAL-SIDED INTERHEMISPHERIC SUBDURAL ELECTRODES, GRID SUBDURAL ELECTRODES, INTRAOPERATIVE SUBDURAL ELECTRODES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053363
510(k) Type
Abbreviated
Applicant
AD-TECH MEDICAL INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2006
Days to Decision
179 days
Submission Type
Summary

DUAL-SIDED INTERHEMISPHERIC SUBDURAL ELECTRODES, GRID SUBDURAL ELECTRODES, INTRAOPERATIVE SUBDURAL ELECTRODES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053363
510(k) Type
Abbreviated
Applicant
AD-TECH MEDICAL INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2006
Days to Decision
179 days
Submission Type
Summary