FDA applicant

Sunbeam Appliance Service Co.

Downers Grove, IL1 decision1987–19870 recalls

FDA records 1 decision for Sunbeam Appliance Service Co. (Downers Grove, IL) in 1987: 1 510(k) clearance. All are in product code KFZ (Humidifier, Non-Direct Patient Interface…). 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, anesthesiology panel, where it files most

How often FDA has decided Sunbeam Appliance Service Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sunbeam Appliance Service Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Sunbeam Appliance Service Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Sunbeam Appliance Service Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Sunbeam”

FDA records each applicant name separately; these may or may not be the same firm.

Sunbeam Corp. 3 Sunbeam Health Division 2 Sunbeam-Oster Household Products 1

Sunbeam Appliance Service Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Sunbeam”