FDA Clearance
LOGIQ Vita; LOGIQ Vita Pro; LOGIQ Vita Express; LOGIQ Vita Plus; LOGIQ Vita Power; LOGIQ S20; LOGIQ S20 Pro; LOGIQ S20 Express; LOGIQ S20 Plus; LOGIQ S20 Power
- Submission
- K260673
- Type
- 510(k)
- Company
- GE Medical Systems Ultrasound and Primary Care Diagnostics
- Decision Date
- Mar 24, 2026
- Specialty
- Radiology
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Source: https://healthaicentral.com/research/regulatory-clearance/clearances/K260673