EAST VENTILARM PRESSURE MONITOR ALARM S.
K-Number: K812960 · 1981-11-16
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Device Summary
Frequently Asked Questions
What is the EAST VENTILARM PRESSURE MONITOR ALARM S.?
EAST VENTILARM PRESSURE MONITOR ALARM S. is a medical device that received FDA 510(k) clearance on 1981-11-16. The listed applicant is Cairco , Ltd.. The 510(k) number is K812960.
When did EAST VENTILARM PRESSURE MONITOR ALARM S. receive FDA 510(k) clearance?
EAST VENTILARM PRESSURE MONITOR ALARM S. received FDA 510(k) clearance on 1981-11-16, under 510(k) number K812960.
Who is the listed applicant for EAST VENTILARM PRESSURE MONITOR ALARM S.?
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 EAST VENTILARM PRESSURE MONITOR ALARM S.?
The FDA product code for EAST VENTILARM PRESSURE MONITOR ALARM S. is CAP.
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: CAP)
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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