AIRVO SERIES HUMIDIFIERS
K-Number: K092846 · 2010-01-27
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Device Summary
Frequently Asked Questions
What is the AIRVO SERIES HUMIDIFIERS?
AIRVO SERIES HUMIDIFIERS is a medical device that received FDA 510(k) clearance on 2010-01-27. The listed applicant is Fisher & Paykel Healthcare, Ltd.. The 510(k) number is K092846.
When did AIRVO SERIES HUMIDIFIERS receive FDA 510(k) clearance?
AIRVO SERIES HUMIDIFIERS received FDA 510(k) clearance on 2010-01-27, under 510(k) number K092846.
Who is the listed applicant for AIRVO SERIES HUMIDIFIERS?
The FDA 510(k) record lists Fisher & Paykel Healthcare, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AIRVO SERIES HUMIDIFIERS?
The FDA product code for AIRVO SERIES HUMIDIFIERS is BTT.
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 Fisher & Paykel Healthcare, Ltd. 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: BTT)
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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