ADULT ANESTHESIA BREATHING CIRCUITS . .
K-Number: K800498 · 1980-03-25
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Device Summary
Frequently Asked Questions
What is the ADULT ANESTHESIA BREATHING CIRCUITS . .?
ADULT 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 K800498.
When did ADULT ANESTHESIA BREATHING CIRCUITS . . receive FDA 510(k) clearance?
ADULT ANESTHESIA BREATHING CIRCUITS . . received FDA 510(k) clearance on 1980-03-25, under 510(k) number K800498.
Who is the listed applicant for ADULT 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 ADULT ANESTHESIA BREATHING CIRCUITS . .?
The FDA product code for ADULT 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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