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NEUROLINE, DISPOSABLE REFERENCE AND RECORDING ELECTRODES TYPE NO: 72000-S, 72010-K

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970639
510(k) Type
Traditional
Applicant
MEDICOTEST, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/1997
Days to Decision
84 days
Submission Type
Statement

NEUROLINE, DISPOSABLE REFERENCE AND RECORDING ELECTRODES TYPE NO: 72000-S, 72010-K

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970639
510(k) Type
Traditional
Applicant
MEDICOTEST, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/1997
Days to Decision
84 days
Submission Type
Statement