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Cleaner, Air, Medical Recirculating

FDA product code FRF · Class 2 · General Hospital

44

Registered devices

31

Adverse events

1

Recalls

53

510(k) clearances

Devices with this code

RGF-BioControls — RGF ENVIRONMENTAL GROUP, INC.Airsonett AIR-4 A-1100 — Airsonett AB RGF-BioControls — RGF ENVIRONMENTAL GROUP, INC.RGF-BioControls — RGF ENVIRONMENTAL GROUP, INC.RGF-BioControls — RGF ENVIRONMENTAL GROUP, INC.HEPA-CARE® — ABATEMENT TECHNOLOGIES, INC.Hepa-Care® — ABATEMENT TECHNOLOGIES, INC.Hepa-Care® — ABATEMENT TECHNOLOGIES, INC.RGF-BioControls — RGF ENVIRONMENTAL GROUP, INC.Hepa-Care® — ABATEMENT TECHNOLOGIES, INC.Hepa-Care® — ABATEMENT TECHNOLOGIES, INC.HEPA-CARE® — ABATEMENT TECHNOLOGIES, INC.Hepa-Care® — ABATEMENT TECHNOLOGIES, INC.Hepa-Care® — ABATEMENT TECHNOLOGIES, INC.Tri-Kleen — TRI-DIM FILTER CORPORATION TRI-KLEEN — TRI-DIM FILTER CORPORATION Hepa-Care® — ABATEMENT TECHNOLOGIES, INC.Hepa-Care® — ABATEMENT TECHNOLOGIES, INC.Hepa-Care® — ABATEMENT TECHNOLOGIES, INC.Hepa-Care® — ABATEMENT TECHNOLOGIES, INC.Hepa-Care® — ABATEMENT TECHNOLOGIES, INC.HEPA-CARE® — ABATEMENT TECHNOLOGIES, INC.RGF-BioControls — RGF ENVIRONMENTAL GROUP, INC.Hepa-Care® — ABATEMENT TECHNOLOGIES, INC.

Recent recalls

Date	Firm	Reason
2012-01-09	Healthway Home Products, Inc.	The Company is recalling certain serial numbers of HealthWay Model 20600-3 and CleanStation Model CS20000 air purifiers because of a potential risk of electrica

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.