Moore Park Mask
K-Number: K183512 · 2019-05-07
Device Summary
Frequently Asked Questions
What is the Moore Park Mask?
Moore Park Mask is a medical device that received FDA 510(k) clearance on 2019-05-07. The listed applicant is Resmed, Ltd.. The 510(k) number is K183512.
When did Moore Park Mask receive FDA 510(k) clearance?
Moore Park Mask received FDA 510(k) clearance on 2019-05-07, under 510(k) number K183512.
Who is the listed applicant for Moore Park 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 Moore Park Mask?
The FDA product code for Moore Park 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.