510(k) Report

FDA applicant

General Anaesthetic Services Limited

Keighley, West Yorkshire, GB1 decision2005–20050 recalls

FDA records 1 decision for General Anaesthetic Services Limited (Keighley, West Yorkshire, GB) in 2005: 1 510(k) clearance. All are in product code CAD (Vaporizer, Anesthesia, Non-Heated). 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, anesthesiology panel, where it files most

How often FDA has decided General Anaesthetic Services Limited’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for General Anaesthetic Services Limited since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like General Anaesthetic Services Limited’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?

  • CADVaporizer, Anesthesia, Non-Heated1decision

Whose devices does it build on?

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

What has FDA decided for it lately?

  • K051666Gav - General Anaesthetic VaporizerGeneral Anaesthetic Services Limited · 2005

The one decision as General Anaesthetic Services Limited →