510(k) Report

FDA applicant

Abatement Technologies, Inc.

Duluth, GA1 decision1999–19990 recalls

FDA records 1 decision for Abatement Technologies, Inc. (Duluth, GA) in 1999: 1 510(k) clearance. All are in product code FRF (Cleaner, Air, Medical Recirculating). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Abatement Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Abatement Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Abatement Technologies, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • FRFCleaner, Air, Medical Recirculating1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K984116Hepa-Care Air Cleaner American Air Filter Air Filtration System Models HC800F, HFS800F, HC800C/ HFS800C…Abatement Technologies, Inc. · 19991cites it

What has FDA decided for it lately?

  • K984116Hepa-Care Air Cleaner American Air Filter Air Filtration System Models HC800F, HFS800F, HC800C/ HFS800C…Abatement Technologies, Inc. · 1999

The one decision as Abatement Technologies, Inc. →