MIRAGE ACTIVA MASK
K-Number: K032916 · 2003-12-04
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Device Summary
Frequently Asked Questions
What is the MIRAGE ACTIVA MASK?
MIRAGE ACTIVA MASK is a medical device that received FDA 510(k) clearance on 2003-12-04. The listed applicant is Resmed, Ltd.. The 510(k) number is K032916.
When did MIRAGE ACTIVA MASK receive FDA 510(k) clearance?
MIRAGE ACTIVA MASK received FDA 510(k) clearance on 2003-12-04, under 510(k) number K032916.
Who is the listed applicant for MIRAGE ACTIVA MASK?
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 ACTIVA MASK?
The FDA product code for MIRAGE ACTIVA MASK 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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