K251659
- 510(k) number
- K251659
- Device name
- Mesh Nebulizer (H6)
- Applicant
- Qingdao Future Medical Technology Co., Ltd. CN
- Product code
- CAF — Nebulizer (Direct Patient Interface)
- Decision date
- 2025-11-14
- Date received
- 2025-05-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K251659.pdf
Official FDA record: K251659
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.