K232588
- 510(k) number
- K232588
- Device name
- Aluna 2
- Applicant
- Knox Medical Diagnostics CA · US
- Product code
- BZH — Meter, Peak Flow, Spirometry
- Decision date
- 2024-11-25
- Date received
- 2023-08-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K232588.pdf
Official FDA record: K232588
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.