AirMax Procedure Mask
K-Number: K211275 · 2021-05-25
Device Summary
Frequently Asked Questions
What is the AirMax Procedure Mask?
AirMax Procedure Mask is a medical device that received FDA 510(k) clearance on 2021-05-25. The listed applicant is Premiumestore, LLC. The 510(k) number is K211275.
When did AirMax Procedure Mask receive FDA 510(k) clearance?
AirMax Procedure Mask received FDA 510(k) clearance on 2021-05-25, under 510(k) number K211275.
Who is the listed applicant for AirMax Procedure Mask?
The FDA 510(k) record lists Premiumestore, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AirMax Procedure Mask?
The FDA product code for AirMax Procedure Mask is FXX.
Other records listing Premiumestore, LLC 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: FXX)
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.