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FDA 510(k)

VENTILATOR ELBOW W/SUCTION PORT

K-Number: K790155 · 1979-02-01

ApplicantAirlife, Inc.
Decision Date1979-02-01
Product CodeBZA
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENTILATOR ELBOW W/SUCTION PORT is the device name listed in this FDA 510(k) record. The listed applicant is Airlife, Inc.. It received FDA 510(k) clearance on 1979-02-01 under 510(k) number K790155. 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 VENTILATOR ELBOW W/SUCTION PORT?

VENTILATOR ELBOW W/SUCTION PORT is a medical device that received FDA 510(k) clearance on 1979-02-01. The listed applicant is Airlife, Inc.. The 510(k) number is K790155.

When did VENTILATOR ELBOW W/SUCTION PORT receive FDA 510(k) clearance?

VENTILATOR ELBOW W/SUCTION PORT received FDA 510(k) clearance on 1979-02-01, under 510(k) number K790155.

Who is the listed applicant for VENTILATOR ELBOW W/SUCTION PORT?

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 VENTILATOR ELBOW W/SUCTION PORT?

The FDA product code for VENTILATOR ELBOW W/SUCTION PORT 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.

View all 76 devices →

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

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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