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AMPLIFIER OTRONA, MODEL N3A-EMG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K772102
510(k) Type
Traditional
Applicant
HONEYWELL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/1977
Days to Decision
14 days

AMPLIFIER OTRONA, MODEL N3A-EMG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K772102
510(k) Type
Traditional
Applicant
HONEYWELL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/1977
Days to Decision
14 days