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TINNITUS AID, MODEL S244

Page Type
Cleared 510(K)
510(k) Number
K770938
510(k) Type
Traditional
Applicant
VICON INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/1977
Days to Decision
36 days

TINNITUS AID, MODEL S244

Page Type
Cleared 510(K)
510(k) Number
K770938
510(k) Type
Traditional
Applicant
VICON INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/1977
Days to Decision
36 days