510(k) Report

FDA applicant

Bonso Electronics International, Inc.

Washington, DC1 decision2003–20030 recalls

FDA records 1 decision for Bonso Electronics International, Inc. (Washington, DC) in 2003: 1 510(k) clearance. All are in product code MNW (Analyzer, Body Composition). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Bonso Electronics International, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bonso Electronics International, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Bonso Electronics International, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Bonso Electronics International, Inc.’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

Which product codes does it file in?

  • MNWAnalyzer, Body Composition1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K030349Healthometer Professional Body Fat Monitor and Scale, Models BFM 940, BFM 945 & BFM 960Bonso Electronics International, Inc. · 20031cites it

What has FDA decided for it lately?

  • K030349Healthometer Professional Body Fat Monitor and Scale, Models BFM 940, BFM 945 & BFM 960Bonso Electronics International, Inc. · 2003

The one decision as Bonso Electronics International, Inc. →