Medical Device Manufacturer · US , Minneapolis , MN

Ototech, Ltd. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1991
4
Total
4
Cleared
0
Denied

Ototech, Ltd. has 4 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 4 cleared submissions from 1991 to 1991. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Ototech, Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ototech, Ltd.

4 devices
1-4 of 4
Cleared Mar 18, 1991
ABRA MODEL LINE LOW DRAIN CUST IN-THE-EAR HEAR AID
K910311 · ESD
Ear, Nose, Throat · 53d
Cleared Mar 18, 1991
C ABRA MODEL LINEAR, LOW DRAIN CUST CANAL HEAR AID
K910312 · ESD
Ear, Nose, Throat · 53d
Cleared Mar 18, 1991
ABRA IPC MODEL INPUT COMPRES AGCCUST ITE HEAR AID
K910313 · ESD
Ear, Nose, Throat · 53d
Cleared Mar 18, 1991
C ABRA MODEL LINEAR, LOW DR. CUSTOM CANAL HEAR AID
K910314 · ESD
Ear, Nose, Throat · 53d
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All4 Ear, Nose, Throat 4