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FDA 510(k)

RADCLIFFE VENTILATOR MARK 5

K-Number: K812953 · 1981-11-27

ApplicantCairco , Ltd.
Decision Date1981-11-27
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RADCLIFFE VENTILATOR MARK 5 is the device name listed in this FDA 510(k) record. The listed applicant is Cairco , Ltd.. It received FDA 510(k) clearance on 1981-11-27 under 510(k) number K812953. 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 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.

View all 9 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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