510(k) Report

FDA applicant

Bawmed UK

United Kingdom, GB2 decisions2004–20040 recalls

FDA records 2 decisions for Bawmed UK (United Kingdom, GB) in 2004: 2 510(k) clearances. Most are in product codes CBP (Valve, Non-Rebreathing) and BTM (Ventilator, Emergency, Manual (Resuscitator)). 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 Bawmed UK’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bawmed UK since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • CBPValve, Non-Rebreathing1decision
  • BTMVentilator, Emergency, Manual (Resuscitator)1decision

What has FDA decided for it lately?

  • K031431Bawmed Rescue MaskBawmed UK · 2004
  • K031434Bawmed E-Z Bag ResuscitatorBawmed UK · 2004

All 2 as Bawmed UK →