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SUBDERMAL NEEDLE ELECTRODE FOR ELECTROENCEPHALOGRAPHY, MODELS PRO-E12SAF AND DEN-12SAF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020910
510(k) Type
Traditional
Applicant
THE ELECTRODE STORE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2002
Days to Decision
121 days
Submission Type
Statement

SUBDERMAL NEEDLE ELECTRODE FOR ELECTROENCEPHALOGRAPHY, MODELS PRO-E12SAF AND DEN-12SAF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020910
510(k) Type
Traditional
Applicant
THE ELECTRODE STORE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2002
Days to Decision
121 days
Submission Type
Statement