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FDA 510(k)

CIRCUIT, BREATHING (W/ CONNECTOR, ADAPT,

K-Number: K792047 · 1979-10-30

ApplicantAirlife, Inc.
Decision Date1979-10-30
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CIRCUIT, BREATHING (W/ CONNECTOR, ADAPT, is the device name listed in this FDA 510(k) record. The listed applicant is Airlife, Inc.. It received FDA 510(k) clearance on 1979-10-30 under 510(k) number K792047. The device is classified under product code BZO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIRCUIT, BREATHING (W/ CONNECTOR, ADAPT,?

CIRCUIT, BREATHING (W/ CONNECTOR, ADAPT, is a medical device that received FDA 510(k) clearance on 1979-10-30. The listed applicant is Airlife, Inc.. The 510(k) number is K792047.

When did CIRCUIT, BREATHING (W/ CONNECTOR, ADAPT, receive FDA 510(k) clearance?

CIRCUIT, BREATHING (W/ CONNECTOR, ADAPT, received FDA 510(k) clearance on 1979-10-30, under 510(k) number K792047.

Who is the listed applicant for CIRCUIT, BREATHING (W/ CONNECTOR, ADAPT,?

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 CIRCUIT, BREATHING (W/ CONNECTOR, ADAPT,?

The FDA product code for CIRCUIT, BREATHING (W/ CONNECTOR, ADAPT, is BZO.

Related Clinical Trials

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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.

K834570VOLUME VENTILATOR CIRCUIT W/WATER TRAPK834573AQUA TRAPK834077SINGLE USE NEBULIZER-ADJUST-AIR ENTRAINK833196VOLUME VENTILATOR CIRCUIT-NEBULIZERK833197TRACH SWIVE/CONNECTORK832725DUAL DIAL VENTURI STYLE MASK

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Related Devices (Code: BZO)

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.

K953784UNICOR, INC. CORRUGATED TUBINGUnicor, Inc.K953785UNICOR, INC. VENTILATOR HOSESUnicor, Inc.K952011PRIMA BREATHING BAGSPrima, Inc.K952022PRIMA VOLUMN VENTILATORSSPrima, Inc.K952010PRIMA VENTILATOR HOSESPrima, Inc.K952012PRIMA CUSTOM ANESTESIA CIRCUITPrima, 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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