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FDA 510(k)

BIRD MEAN AIRWAY PRESSURE MONITOR

K-Number: K812140 · 1981-08-20

Applicant3M Company
Decision Date1981-08-20
Product CodeCAP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BIRD MEAN AIRWAY PRESSURE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is 3M Company. It received FDA 510(k) clearance on 1981-08-20 under 510(k) number K812140. 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 BIRD MEAN AIRWAY PRESSURE MONITOR?

BIRD MEAN AIRWAY PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 1981-08-20. The listed applicant is 3M Company. The 510(k) number is K812140.

When did BIRD MEAN AIRWAY PRESSURE MONITOR receive FDA 510(k) clearance?

BIRD MEAN AIRWAY PRESSURE MONITOR received FDA 510(k) clearance on 1981-08-20, under 510(k) number K812140.

Who is the listed applicant for BIRD MEAN AIRWAY PRESSURE MONITOR?

The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIRD MEAN AIRWAY PRESSURE MONITOR?

The FDA product code for BIRD MEAN AIRWAY PRESSURE MONITOR 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 3M Company 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.

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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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