Home › ABATEMENT TECHNOLOGIES, INC. › Hepa-Care®
Hepa-Care®
ABATEMENT TECHNOLOGIES, INC. · Model HC800C · UDI-DI 00818261020909
1
510(k) clearances
31
Adverse events
1
Recalls
11
Facilities
Description
Hepa-Care® Ceiling Unit, 115 Volt, 3 Amp, 60 Hz. Motor thermally protected single phase. Electrical Safety: CAN/CSA C22.2 No. 113:2015-05 & UL 507:1999/R2012-06. Mechanical safety: CAN/CSA C22.2 No. 113:2015-05 & UL 507:1999/R2012-06. Made in Canada
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 electrical arcing that could |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.