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FDA 510(k)

AV-S ANAESTHESIA VENTILATOR

K-Number: K051222 · 2005-09-23

Decision Date2005-09-23
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AV-S ANAESTHESIA VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Penlon Limited. It received FDA 510(k) clearance on 2005-09-23 under 510(k) number K051222. 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 AV-S ANAESTHESIA VENTILATOR?

AV-S ANAESTHESIA VENTILATOR is a medical device that received FDA 510(k) clearance on 2005-09-23. The listed applicant is Penlon Limited. The 510(k) number is K051222.

When did AV-S ANAESTHESIA VENTILATOR receive FDA 510(k) clearance?

AV-S ANAESTHESIA VENTILATOR received FDA 510(k) clearance on 2005-09-23, under 510(k) number K051222.

Who is the listed applicant for AV-S ANAESTHESIA VENTILATOR?

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

What is the FDA product code for AV-S ANAESTHESIA VENTILATOR?

The FDA product code for AV-S ANAESTHESIA 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 Penlon Limited 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.

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

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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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