CM 5000R REMOTE AIRWAY PRESSURE
K-Number: K873953 · 1987-10-27
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Device Summary
Frequently Asked Questions
What is the CM 5000R REMOTE AIRWAY PRESSURE?
CM 5000R REMOTE AIRWAY PRESSURE is a medical device that received FDA 510(k) clearance on 1987-10-27. The listed applicant is Canadian Monaghan , Ltd.. The 510(k) number is K873953.
When did CM 5000R REMOTE AIRWAY PRESSURE receive FDA 510(k) clearance?
CM 5000R REMOTE AIRWAY PRESSURE received FDA 510(k) clearance on 1987-10-27, under 510(k) number K873953.
Who is the listed applicant for CM 5000R REMOTE AIRWAY PRESSURE?
The FDA 510(k) record lists Canadian Monaghan , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CM 5000R REMOTE AIRWAY PRESSURE?
The FDA product code for CM 5000R REMOTE AIRWAY PRESSURE 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 Canadian Monaghan , 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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