Medical Device Manufacturer · US , Mchenry , IL

Vicon Instrument Co. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1976
8
Total
8
Cleared
0
Denied

Vicon Instrument Co. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 8 cleared submissions from 1976 to 1981. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Vicon Instrument Co. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Vicon Instrument Co.

8 devices
1-8 of 8
Cleared Jul 15, 1981
FINETONE MODEL VI HEARING AID
K811751 · ESD
Ear, Nose, Throat · 23d
Cleared Aug 03, 1979
SCREENING AUDIOMETER, HIGH FREQUENCY
K790878 · EWO
Ear, Nose, Throat · 88d
Cleared Feb 16, 1979
TINNITUS DEVICES
K790064 · ETS
Ear, Nose, Throat · 32d
Cleared Jan 03, 1978
TINNITUS MASKERS, MODELS S564&S574
K771769 · KLW
Ear, Nose, Throat · 106d
Cleared Oct 04, 1977
MODULAR HEARING DEVICE, MODEL S291
K771762 · ESD
Ear, Nose, Throat · 15d
Cleared Jun 28, 1977
TINNITUS AID, MODEL S244
K770938 · KLW
Ear, Nose, Throat · 36d
Cleared Dec 16, 1976
HEARING AIDS (MODEL E-552 S-712)
K761216 · ESD
Ear, Nose, Throat · 9d
Cleared Jul 21, 1976
HEARING AID, S-522 FM
K760215 · ESD
Ear, Nose, Throat · 9d
Filters
Filter by Specialty
All8 Ear, Nose, Throat 8