Abatement Technologies, Inc. is one of 7976 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Abatement Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: HEPA-CARE AIR CLEANER AMERICAN AIR FILTER AIR FILTRATION SYSTEM MODELS HC800F, HFS800F, HC800C/ HFS800C, HC400C/HFS400C
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