FDA Clearance
HERA Z20, R20, HERA Z30, R30 Diagnostic Ultrasound System
- Submission
- K241971
- Type
- 510(k)
- Company
- Samsung Medison Co., Ltd.
- Decision Date
- Oct 11, 2024
- Specialty
- Radiology
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Source: https://healthaicentral.com/research/regulatory-clearance/clearances/K241971