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FDA 510(k)

MASK INTULATION ADAPTOR

K-Number: K790149 · 1979-02-01

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

Device Summary

MASK INTULATION 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 1979-02-01 under 510(k) number K790149. 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 MASK INTULATION ADAPTOR?

MASK INTULATION ADAPTOR 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 K790149.

When did MASK INTULATION ADAPTOR receive FDA 510(k) clearance?

MASK INTULATION ADAPTOR received FDA 510(k) clearance on 1979-02-01, under 510(k) number K790149.

Who is the listed applicant for MASK INTULATION 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 MASK INTULATION ADAPTOR?

The FDA product code for MASK INTULATION 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.

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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.

K834573AQUA TRAPK834570VOLUME VENTILATOR CIRCUIT W/WATER TRAPK834077SINGLE USE NEBULIZER-ADJUST-AIR ENTRAINK833196VOLUME VENTILATOR CIRCUIT-NEBULIZERK833197TRACH SWIVE/CONNECTORK832725DUAL DIAL VENTURI STYLE MASK

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.

K083702TRACH-ASSISTMergenet MedicalK954383SURELOC CIRCUIT CONNECTORPolamedco, Inc.K954197DISPOSABLE FLEX TUBEEngstrom MedicalK953786UNICOR, INC. CONNECTORS & AIRWAY EXTENSIONSUnicor, Inc.K952824NEO-LINK, DISPOSABLE NEONATAL AIR WAY CONNECTORIntertex Medical, Inc.K951345DISPOSABLE AIRWAY CONNECTORS FOR GAS SAMPLINGCatheter Research, Inc.

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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