Medical Device Manufacturer · US , Bend , OR

Mini-Mitter Co., Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1999
5
Total
5
Cleared
0
Denied

Mini-Mitter Co., Inc. has 5 FDA 510(k) cleared medical devices. Based in Bend, US.

Historical record: 5 cleared submissions from 1999 to 2004. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Mini-Mitter Co., Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Mini-Mitter Co., Inc.

5 devices
1-5 of 5
Filters