K242467
- 510(k) number
- K242467
- Device name
- IQ-UIP
- Applicant
- Imbio, Inc. MN · US
- Product code
- QWO — Radiology Software For Referral Of Findings Related
- Decision date
- 2024-12-19
- Date received
- 2024-08-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K242467.pdf
Official FDA record: K242467
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.