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Vicon Instrument Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K811751FINETONE MODEL VI HEARING AIDJuly 15, 1981
K790878SCREENING AUDIOMETER, HIGH FREQUENCYAugust 3, 1979
K790064TINNITUS DEVICESFebruary 16, 1979
K771769TINNITUS MASKERS, MODELS S564&S574January 3, 1978
K771762MODULAR HEARING DEVICE, MODEL S291October 4, 1977
K770938TINNITUS AID, MODEL S244June 28, 1977
K761216HEARING AIDS (MODEL E-552 S-712)December 16, 1976
K760215HEARING AID, S-522 FMJuly 21, 1976