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FDA 510(k)

INSPIRATORY FORCE PRESSURE ADAPTOR

K-Number: K812067 · 1981-08-12

ApplicantAirlife, Inc.
Decision Date1981-08-12
Product CodeBZA
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INSPIRATORY FORCE PRESSURE ADAPTOR is the device name listed in this FDA 510(k) record. The listed applicant is Airlife, Inc.. It received FDA 510(k) clearance on 1981-08-12 under 510(k) number K812067. The device is classified under product code BZA. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSPIRATORY FORCE PRESSURE ADAPTOR?

INSPIRATORY FORCE PRESSURE ADAPTOR is a medical device that received FDA 510(k) clearance on 1981-08-12. The listed applicant is Airlife, Inc.. The 510(k) number is K812067.

When did INSPIRATORY FORCE PRESSURE ADAPTOR receive FDA 510(k) clearance?

INSPIRATORY FORCE PRESSURE ADAPTOR received FDA 510(k) clearance on 1981-08-12, under 510(k) number K812067.

Who is the listed applicant for INSPIRATORY FORCE PRESSURE ADAPTOR?

The FDA 510(k) record lists Airlife, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSPIRATORY FORCE PRESSURE ADAPTOR?

The FDA product code for INSPIRATORY FORCE PRESSURE ADAPTOR is BZA.

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 Airlife, Inc. 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: BZA)

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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