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FDA 510(k)

CM 5000 MONITOR AIRWAY PRESSURE

K-Number: K871083 · 1987-04-08

Decision Date1987-04-08
Product CodeCAP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CM 5000 MONITOR AIRWAY PRESSURE is the device name listed in this FDA 510(k) record. The listed applicant is Canadian Monaghan , Ltd.. It received FDA 510(k) clearance on 1987-04-08 under 510(k) number K871083. The device is classified under product code CAP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CM 5000 MONITOR AIRWAY PRESSURE?

CM 5000 MONITOR AIRWAY PRESSURE is a medical device that received FDA 510(k) clearance on 1987-04-08. The listed applicant is Canadian Monaghan , Ltd.. The 510(k) number is K871083.

When did CM 5000 MONITOR AIRWAY PRESSURE receive FDA 510(k) clearance?

CM 5000 MONITOR AIRWAY PRESSURE received FDA 510(k) clearance on 1987-04-08, under 510(k) number K871083.

Who is the listed applicant for CM 5000 MONITOR 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 5000 MONITOR AIRWAY PRESSURE?

The FDA product code for CM 5000 MONITOR 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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