Medical Device Manufacturer · US , Duluth , GA

Abatement Technologies, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1999
1
Total
1
Cleared
0
Denied

Abatement Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Duluth, US.

Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Abatement Technologies, Inc.

1 devices
1-1 of 1
Filters
All1 General Hospital 1