K232186
- 510(k) number
- K232186
- Device name
- LOGIQ e
- Applicant
- Ge Medical Systems Ultrasound and Primary Care Diagnostic, WI · US
- Product code
- IYN — System, Imaging, Pulsed Doppler, Ultrasonic
- Decision date
- 2023-11-03
- Date received
- 2023-07-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K232186.pdf
Official FDA record: K232186
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.