MIRAGE FULL FACE MASK SERIES 2
K-Number: K023306 · 2002-11-27
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Device Summary
Frequently Asked Questions
What is the MIRAGE FULL FACE MASK SERIES 2?
MIRAGE FULL FACE MASK SERIES 2 is a medical device that received FDA 510(k) clearance on 2002-11-27. The listed applicant is Resmed, Ltd.. The 510(k) number is K023306.
When did MIRAGE FULL FACE MASK SERIES 2 receive FDA 510(k) clearance?
MIRAGE FULL FACE MASK SERIES 2 received FDA 510(k) clearance on 2002-11-27, under 510(k) number K023306.
Who is the listed applicant for MIRAGE FULL FACE MASK SERIES 2?
The FDA 510(k) record lists Resmed, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MIRAGE FULL FACE MASK SERIES 2?
The FDA product code for MIRAGE FULL FACE MASK SERIES 2 is BZD.
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 Resmed, 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: BZD)
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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