Modulus Verni-Trol Anesthetic Vaporizer

FDA 510(k) K821966 · Ohio Medical Products

Substantially Equivalent

510(k) numberK821966

Submission

Device name
Modulus Verni-Trol Anesthetic Vaporizer
Applicant
Ohio Medical Products
Mchenry, IL, US
Received
July 2, 1982
Decision date
July 16, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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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
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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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Questions and answers

When was Modulus Verni-Trol Anesthetic Vaporizer cleared by the FDA?

Modulus Verni-Trol Anesthetic Vaporizer (K821966) received a 510(k) decision of Substantially Equivalent on July 16, 1982, 14 days after the submission was received.

What is the product code of K821966?

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