Datex-Ohmeda D-Tec Plus Anesthesia Vaporizer

FDA 510(k) K002878 · Datex-Ohmeda, Inc.

Substantially Equivalent

510(k) numberK002878

Submission

Device name
Datex-Ohmeda D-Tec Plus Anesthesia Vaporizer
Applicant
Datex-Ohmeda, Inc.
Madison, WI, US
Received
September 15, 2000
Decision date
September 21, 2000
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

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

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K240375V80 Anesthetic Vaporizer (V80)CAD · Traditional Shenzhen Mindray Bio-Medical Electronics Co., Ltd.10/31/2024SE
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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
K051666Gav - General Anaesthetic VaporizerCAD · Traditional General Anaesthetic Services Limited08/23/2005SE
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

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K210384Carescape R860CBK · Traditional 11/04/2021SE
K172702Tec 820, Tec 850CAD · Traditional 01/04/2018SE
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Questions and answers

When was Datex-Ohmeda D-Tec Plus Anesthesia Vaporizer cleared by the FDA?

Datex-Ohmeda D-Tec Plus Anesthesia Vaporizer (K002878) received a 510(k) decision of Substantially Equivalent on September 21, 2000, 6 days after the submission was received.

What is the product code of K002878?

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