Gav - General Anaesthetic Vaporizer

FDA 510(k) K051666 · General Anaesthetic Services Limited

Substantially Equivalent

510(k) numberK051666

Submission

Device name
Gav - General Anaesthetic Vaporizer
Applicant
General Anaesthetic Services Limited
Keighley, West Yorkshire, GB
Received
June 22, 2005
Decision date
August 23, 2005
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

Official FDA 510(k) record

Device classification

Product code
CAD – Vaporizer, Anesthesia, Non-Heated
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5880
Specialty
Anesthesiology

Other 510(k)s with product code CAD

510(k)DeviceApplicantDecision
K240375V80 Anesthetic Vaporizer (V80)CAD · Traditional Shenzhen Mindray Bio-Medical Electronics Co., Ltd.10/31/2024SE
K172702Tec 820, Tec 850CAD · Traditional Datex-Ohmeda, Inc.01/04/2018SE
K150167V60 Anesthetic VaporizerCAD · Traditional Shenzhen Mindray Bio-Medical Electronics Co., Ltd.06/30/2015SE
K110608Sevoflurane Vaporizer AdaptorCAD · Traditional Piramal Critcal Care, Inc (Formerly Minrad, Inc)07/20/2011SE
K060331Sigma Alpha VaporizerCAD · Traditional Penlon Limited05/10/2006SE
K053564Keyed Filler Bottle Adaptor, Models 53450, 53452, 53453, 53454CAD · Traditional Penlon Limited03/03/2006SE
K042276D-VaporCAD · Traditional Draeger Medical, Inc.09/23/2004SE
K041076Delta TCAD · Special Penlon , Ltd.08/09/2004SE
K031027Datex-Ohmeda Tec 7 Anesthesia Vaporizer (Enflurane)CAD · Special Datex-Ohmeda, Inc.06/26/2003SE
K012924Datex-Ohmeda Tec 7 Anesthesia VaporizerCAD · Special Datex-Ohmeda, Inc.01/30/2002SE

Questions and answers

When was Gav - General Anaesthetic Vaporizer cleared by the FDA?

Gav - General Anaesthetic Vaporizer (K051666) received a 510(k) decision of Substantially Equivalent on August 23, 2005, 62 days after the submission was received.

What is the product code of K051666?

The FDA product code is CAD – Vaporizer, Anesthesia, Non-Heated, a Class II (moderate risk) device regulated under 21 CFR 868.5880.