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EPIDURAL PEG ELECTRODE (EP), SPHENOIDAL ELECTRODE (EDS) AND FORAMEN, OVALE DEPTH ELECTRODE (ED-FO) FOR EPILEPSY MONITORI

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961942
510(k) Type
Traditional
Applicant
Radionics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/1997
Days to Decision
455 days
Submission Type
Summary

EPIDURAL PEG ELECTRODE (EP), SPHENOIDAL ELECTRODE (EDS) AND FORAMEN, OVALE DEPTH ELECTRODE (ED-FO) FOR EPILEPSY MONITORI

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961942
510(k) Type
Traditional
Applicant
Radionics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/1997
Days to Decision
455 days
Submission Type
Summary