Ohio V5A Anesthesia Ventilator

FDA 510(k) K822456 · Airco/Ohio Medical Products

Substantially Equivalent

510(k) numberK822456

Submission

Device name
Ohio V5A Anesthesia Ventilator
Applicant
Airco/Ohio Medical Products
Mchenry, IL, US
Received
August 16, 1982
Decision date
September 21, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CBK – Ventilator, Continuous, Facility Use
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5895
Specialty
Anesthesiology
Life-sustaining
Yes

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K830446Oxygen Monitor Ohio 5100CCL · Traditional 03/24/1983SE
K813476Ohio Volume Incentive SpirometerBWF · Traditional 12/31/1981SE
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Questions and answers

When was Ohio V5A Anesthesia Ventilator cleared by the FDA?

Ohio V5A Anesthesia Ventilator (K822456) received a 510(k) decision of Substantially Equivalent on September 21, 1982, 36 days after the submission was received.

What is the product code of K822456?

The FDA product code is CBK – Ventilator, Continuous, Facility Use, a Class II (moderate risk) device regulated under 21 CFR 868.5895.