Mesh Nebulizer (H6)
K-Number: K251659 · 2025-11-14
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.