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FDA 510(k)

GAV - GENERAL ANAESTHETIC VAPORIZER

K-Number: K051666 · 2005-08-23

Decision Date2005-08-23
Product CodeCAD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

GAV - GENERAL ANAESTHETIC VAPORIZER is the device name listed in this FDA 510(k) record. The listed applicant is General Anaesthetic Services Limited. It received FDA 510(k) clearance on 2005-08-23 under 510(k) number K051666. The device is classified under product code CAD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GAV - GENERAL ANAESTHETIC VAPORIZER?

GAV - GENERAL ANAESTHETIC VAPORIZER is a medical device that received FDA 510(k) clearance on 2005-08-23. The listed applicant is General Anaesthetic Services Limited. The 510(k) number is K051666.

When did GAV - GENERAL ANAESTHETIC VAPORIZER receive FDA 510(k) clearance?

GAV - GENERAL ANAESTHETIC VAPORIZER received FDA 510(k) clearance on 2005-08-23, under 510(k) number K051666.

Who is the listed applicant for GAV - GENERAL ANAESTHETIC VAPORIZER?

The FDA 510(k) record lists General Anaesthetic Services Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GAV - GENERAL ANAESTHETIC VAPORIZER?

The FDA product code for GAV - GENERAL ANAESTHETIC VAPORIZER is CAD.

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.

Related Devices (Code: CAD)

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

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

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