PEDIATRIC ANESTHESIA BREATHING CIRCUITS
K-Number: K800499 · 1980-03-25
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Device Summary
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.
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
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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