RADCLIFFE VENTILATOR MARK 5
K-Number: K812953 · 1981-11-27
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Device Summary
Frequently Asked Questions
What is the RADCLIFFE VENTILATOR MARK 5?
RADCLIFFE VENTILATOR MARK 5 is a medical device that received FDA 510(k) clearance on 1981-11-27. The listed applicant is Cairco , Ltd.. The 510(k) number is K812953.
When did RADCLIFFE VENTILATOR MARK 5 receive FDA 510(k) clearance?
RADCLIFFE VENTILATOR MARK 5 received FDA 510(k) clearance on 1981-11-27, under 510(k) number K812953.
Who is the listed applicant for RADCLIFFE VENTILATOR MARK 5?
The FDA 510(k) record lists Cairco , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RADCLIFFE VENTILATOR MARK 5?
The FDA product code for RADCLIFFE VENTILATOR MARK 5 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 Cairco , Ltd. 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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