GAV - GENERAL ANAESTHETIC VAPORIZER— 510(k) K051666

Name: FDA 510(k) clearance K051666
Creator: U.S. Food and Drug Administration
Published: 2005-08-23

Substantially Equivalent

General Anaesthetic Services Limited

FDA 510(k) clearance K051666 for GAV - GENERAL ANAESTHETIC VAPORIZER, Substantially Equivalent on 2005-08-23. Applicant: General Anaesthetic Services Limited. Device class: 2.

Clearance details

Applicant: General Anaesthetic Services Limited
Product code: Code CAD
Device class: Class 2
Regulation: 21 CFR 868.5880
Advisory panel: Anesthesiology
Date received: 2005-06-22
Decision date: 2005-08-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Keighley, West Yorkshire, GB

Download summary PDF View on FDA.gov ↗

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K110608 — SEVOFLURANE VAPORIZER ADAPTOR2011-07-20
K060331 — SIGMA ALPHA VAPORIZER2006-05-10

Adverse events under product code CAD

product code CAD

Malfunction: 3,275
Total: 3,275

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.