Medical Device Manufacturer · US , Mchenry , IL

Finetone Hearing Instruments - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1983
5
Total
5
Cleared
0
Denied

Finetone Hearing Instruments has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 5 cleared submissions from 1983 to 1998. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Finetone Hearing Instruments Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Finetone Hearing Instruments

5 devices
1-5 of 5
Cleared Feb 20, 1998
FACEPLATE ASSEMBLY
K974219 · LRB
Ear, Nose, Throat · 102d
Cleared Feb 02, 1996
FINETONE FSC,
K955692 · ESD
Ear, Nose, Throat · 50d
Cleared Dec 21, 1994
FINETONE DISCEET CANAL
K945780 · ESD
Ear, Nose, Throat · 26d
Cleared Jun 29, 1994
SUPER-SIL
K940164 · ESD
Ear, Nose, Throat · 174d
Cleared Jun 30, 1983
CUSTOM IN-THE-EAR HEARING AID
K830960 · ESD
Ear, Nose, Throat · 97d
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All5 Ear, Nose, Throat 5