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FDA 510(k)

Mesh Nebulizer (H6)

K-Number: K251659 · 2025-11-14

Decision Date2025-11-14
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Mesh Nebulizer (H6) is the device name listed in this FDA 510(k) record. The listed applicant is Qingdao Future Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-11-14 under 510(k) number K251659. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Mesh Nebulizer (H6)?

Mesh Nebulizer (H6) is a medical device that received FDA 510(k) clearance on 2025-11-14. The listed applicant is Qingdao Future Medical Technology Co., Ltd.. The 510(k) number is K251659.

When did Mesh Nebulizer (H6) receive FDA 510(k) clearance?

Mesh Nebulizer (H6) received FDA 510(k) clearance on 2025-11-14, under 510(k) number K251659.

Who is the listed applicant for Mesh Nebulizer (H6)?

The FDA 510(k) record lists Qingdao Future Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Mesh Nebulizer (H6)?

The FDA product code for Mesh Nebulizer (H6) is CAF.

Other records listing Qingdao Future Medical Technology Co., 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: CAF)

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

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