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FDA 510(k)

Airmod

K-Number: K242798 · 2025-02-28

ApplicantHeroic Faith International , Ltd.
Decision Date2025-02-28
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Airmod is the device name listed in this FDA 510(k) record. The listed applicant is Heroic Faith International , Ltd.. It received FDA 510(k) clearance on 2025-02-28 under 510(k) number K242798. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Airmod?

Airmod is a medical device that received FDA 510(k) clearance on 2025-02-28. The listed applicant is Heroic Faith International , Ltd.. The 510(k) number is K242798.

When did Airmod receive FDA 510(k) clearance?

Airmod received FDA 510(k) clearance on 2025-02-28, under 510(k) number K242798.

Who is the listed applicant for Airmod?

The FDA 510(k) record lists Heroic Faith International , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Airmod?

The FDA product code for Airmod is BZQ.

Other records listing Heroic Faith International , 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.

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Related Devices (Code: BZQ)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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