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FDA 510(k)

VS, ANESTHESIA VENTILATOR

K-Number: K790809 · 1979-05-04

Decision Date1979-05-04
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VS, ANESTHESIA VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Airco/Ohio Medical Products. It received FDA 510(k) clearance on 1979-05-04 under 510(k) number K790809. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VS, ANESTHESIA VENTILATOR?

VS, ANESTHESIA VENTILATOR is a medical device that received FDA 510(k) clearance on 1979-05-04. The listed applicant is Airco/Ohio Medical Products. The 510(k) number is K790809.

When did VS, ANESTHESIA VENTILATOR receive FDA 510(k) clearance?

VS, ANESTHESIA VENTILATOR received FDA 510(k) clearance on 1979-05-04, under 510(k) number K790809.

Who is the listed applicant for VS, ANESTHESIA VENTILATOR?

The FDA 510(k) record lists Airco/Ohio Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VS, ANESTHESIA VENTILATOR?

The FDA product code for VS, ANESTHESIA VENTILATOR is CBK.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Airco/Ohio Medical Products as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 13 devices →

Related Devices (Code: CBK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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