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FDA 510(k)

PEDIATRIC ANESTHESIA BREATHING CIRCUITS

K-Number: K800499 · 1980-03-25

ApplicantAirlife, Inc.
Decision Date1980-03-25
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PEDIATRIC ANESTHESIA BREATHING CIRCUITS is the device name listed in this FDA 510(k) record. The listed applicant is Airlife, Inc.. It received FDA 510(k) clearance on 1980-03-25 under 510(k) number K800499. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDIATRIC ANESTHESIA BREATHING CIRCUITS?

PEDIATRIC ANESTHESIA BREATHING CIRCUITS is a medical device that received FDA 510(k) clearance on 1980-03-25. The listed applicant is Airlife, Inc.. The 510(k) number is K800499.

When did PEDIATRIC ANESTHESIA BREATHING CIRCUITS receive FDA 510(k) clearance?

PEDIATRIC ANESTHESIA BREATHING CIRCUITS received FDA 510(k) clearance on 1980-03-25, under 510(k) number K800499.

Who is the listed applicant for PEDIATRIC ANESTHESIA BREATHING CIRCUITS?

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 PEDIATRIC ANESTHESIA BREATHING CIRCUITS?

The FDA product code for PEDIATRIC ANESTHESIA BREATHING CIRCUITS is CAI.

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: CAI)

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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