Pocket Ultrasound System (C10)
FDA 510(k) clearance K231354 · decided 2023-12-20
Clearance details
- K-number
- K231354
- Device name
- Pocket Ultrasound System (C10)
- Applicant
- Beijing Konted Medical Technology Co.,Ltd
- Decision
- Substantially Equivalent
- Date received
- 2023-05-10
- Decision date
- 2023-12-20
- Days to decision
- 224 days
- Clearance type
- Traditional
- Product code
- IYN
- Device class
- 2
- Regulation number
- 892.1550
- Medical specialty
- Radiology
- Advisory committee
- Radiology
- Location
- Beijing, CN
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.