Medical Device Manufacturer · US , Lake Andes , SD

Dakota Laboratories, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1992
1
Total
1
Cleared
0
Denied

Dakota Laboratories, Inc. has 1 FDA 510(k) cleared medical devices. Based in Lake Andes, US.

Historical record: 1 cleared submissions from 1992 to 1992. Primary specialty: Ear, Nose, Throat.

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

FDA 510(k) Regulatory Record - Dakota Laboratories, Inc.

1 devices
1-1 of 1
Cleared Mar 31, 1992
DI CUSTOM IN THE EAR AND IN THE CANAL
K920657 · ESD
Ear, Nose, Throat · 48d
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