FDA Device Recall
Koios DS Breast . The device is a software application which assists skilled physicians in analyzing breast ultrasound…
- Recall Number
- Z-0820-2020
- CFRES ID
- 178820
- Firm
- Koios Medical, Inc.
- Status
- Terminated
- Initiated
- Dec 31, 2019
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Source: https://healthaicentral.com/research/regulatory-clearance/recalls/178820