K240009
- 510(k) number
- K240009
- Device name
- iQFlex Pro
- Applicant
- First Source, Inc. NY · US
- Product code
- IZL — System, X-Ray, Mobile
- Decision date
- 2024-07-03
- Date received
- 2024-01-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K240009.pdf
Official FDA record: K240009
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.