AV-S ANAESTHESIA VENTILATOR
K-Number: K051222 · 2005-09-23
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Device Summary
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
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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