Vicon Instrument Co. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vicon Instrument Co. Ear, Nose, Throat ✕
8 devices
Cleared
Jul 15, 1981
FINETONE MODEL VI HEARING AID
Ear, Nose, Throat
23d
Cleared
Aug 03, 1979
SCREENING AUDIOMETER, HIGH FREQUENCY
Ear, Nose, Throat
88d
Cleared
Feb 16, 1979
TINNITUS DEVICES
Ear, Nose, Throat
32d
Cleared
Jan 03, 1978
TINNITUS MASKERS, MODELS S564&S574
Ear, Nose, Throat
106d
Cleared
Oct 04, 1977
MODULAR HEARING DEVICE, MODEL S291
Ear, Nose, Throat
15d
Cleared
Jun 28, 1977
TINNITUS AID, MODEL S244
Ear, Nose, Throat
36d
Cleared
Dec 16, 1976
HEARING AIDS (MODEL E-552 S-712)
Ear, Nose, Throat
9d
Cleared
Jul 21, 1976
HEARING AID, S-522 FM
Ear, Nose, Throat
9d