FDA applicant

Erie Mfg., Co.

Mchenry, IL1 decision1978–19780 recalls

FDA records 1 decision for Erie Mfg., Co. (Mchenry, IL) in 1978: 1 510(k) clearance. All are in product code CAN (Regulator, Pressure, Gas Cylinder). 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 Erie Mfg., Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Erie Mfg., Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Erie Mfg., 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 “Erie”

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

Erie Medical 5 Erie Scientific Co. 1 Erie Controls 1

Erie Mfg., Co.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Erie”