AIRLIFE HEATED VENTILATOR AND BREATHING CIRCUITS
K-Number: K993833 · 1999-12-10
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Device Summary
Frequently Asked Questions
What is the AIRLIFE HEATED VENTILATOR AND BREATHING CIRCUITS?
AIRLIFE HEATED VENTILATOR AND BREATHING CIRCUITS is a medical device that received FDA 510(k) clearance on 1999-12-10. The listed applicant is Allegiance Healthcare Corp.. The 510(k) number is K993833.
When did AIRLIFE HEATED VENTILATOR AND BREATHING CIRCUITS receive FDA 510(k) clearance?
AIRLIFE HEATED VENTILATOR AND BREATHING CIRCUITS received FDA 510(k) clearance on 1999-12-10, under 510(k) number K993833.
Who is the listed applicant for AIRLIFE HEATED VENTILATOR AND BREATHING CIRCUITS?
The FDA 510(k) record lists Allegiance Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AIRLIFE HEATED VENTILATOR AND BREATHING CIRCUITS?
The FDA product code for AIRLIFE HEATED VENTILATOR AND BREATHING CIRCUITS is BZE.
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 Allegiance Healthcare Corp. 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: BZE)
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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