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SCREENING AUDIOMETER, HIGH FREQUENCY

Page Type
Cleared 510(K)
510(k) Number
K790878
510(k) Type
Traditional
Applicant
VICON INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1979
Days to Decision
88 days

SCREENING AUDIOMETER, HIGH FREQUENCY

Page Type
Cleared 510(K)
510(k) Number
K790878
510(k) Type
Traditional
Applicant
VICON INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1979
Days to Decision
88 days