FDA Clearance
V8 Diagnostic Ultrasound System; cV8 Diagnostic Ultrasound System; V7 Diagnostic Ultrasound System; cV7 Diagnostic Ultrasound System; V6 Diagnostic Ultrasound System; cV6 Diagnostic Ultrasound System; V5 Diagnostic Ultrasound System; cV5 Diagnostic Ultrasound System; V4 Diagnostic Ultrasound System; cV4 Diagnostic Ultrasound System
- Submission
- K250999
- Type
- 510(k)
- Company
- Samsung Medison Co., Ltd.
- Decision Date
- Jul 18, 2025
- Specialty
- Radiology
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Source: https://healthaicentral.com/research/regulatory-clearance/clearances/K250999