FDA applicant

Conway Electronic Enterprises, Ltd.

Mchenry, IL1 decision1976–19760 recalls

FDA records 1 decision for Conway Electronic Enterprises, Ltd. (Mchenry, IL) in 1976: 1 510(k) clearance. All are in product code DPS (Electrocardiograph). 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, cardiovascular panel, where it files most

How often FDA has decided Conway Electronic Enterprises, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Conway Electronic Enterprises, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Conway Electronic Enterprises, Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Conway”

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

Conway Stuart Medical, Inc. 10

Conway Electronic Enterprises, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Conway”