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AMPLIFIER MODEL N3B-EEG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K771683
510(k) Type
Traditional
Applicant
HONEYWELL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/1977
Days to Decision
14 days

AMPLIFIER MODEL N3B-EEG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K771683
510(k) Type
Traditional
Applicant
HONEYWELL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/1977
Days to Decision
14 days