Medical Device Manufacturer · DK , Thisted

Oticon A/S - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1995
2
Total
2
Cleared
0
Denied

Oticon A/S has 2 FDA 510(k) cleared medical devices. Based in Thisted, DK.

Historical record: 2 cleared submissions from 1995 to 2014. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Oticon A/S Filter by specialty or product code using the sidebar.

Oticon A/S — FDA 510(k) Products and Clearance History

2 devices
1-2 of 2
Cleared Mar 18, 2014
TINNITUS SOUNDSUPPORT
K133308 · KLW
Ear, Nose, Throat · 141d
Cleared Sep 18, 1995
AMENDMENTS TO MULTIFOCUS
K951002 · ESD
Ear, Nose, Throat · 203d
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