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 a medical device manufactured by Qingdao Future Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-11-14 under approval 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. It is manufactured by Qingdao Future Medical Technology Co., Ltd.. The 510(k) number is K251659.
When was Mesh Nebulizer (H6) approved by the FDA?
Mesh Nebulizer (H6) received FDA 510(k) clearance on 2025-11-14, under approval number K251659.
What company makes Mesh Nebulizer (H6)?
Mesh Nebulizer (H6) is manufactured by Qingdao Future Medical Technology Co., Ltd..
What is the FDA product code for Mesh Nebulizer (H6)?
The FDA product code for Mesh Nebulizer (H6) is CAF.
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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.