K233998
- 510(k) number
- K233998
- Device name
- TRAQinform IQ
- Applicant
- Aiq Global, Inc. WI · US
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2024-09-05
- Date received
- 2023-12-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K233998.pdf
Official FDA record: K233998
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.