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GOLD CUP EEG CUTANEOUS ELECTRODE W/LEAD AND EXT.

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911989
510(k) Type
Traditional
Applicant
SOMNITEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1991
Days to Decision
85 days
Submission Type
Statement

GOLD CUP EEG CUTANEOUS ELECTRODE W/LEAD AND EXT.

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911989
510(k) Type
Traditional
Applicant
SOMNITEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1991
Days to Decision
85 days
Submission Type
Statement