EVO Q30 Diagnostic Ultrasound System; EVO Q20 Diagnostic Ultrasound System; EVO Q10 Diagnostic Ultrasound System; EVO XQ30 Diagnostic Ultrasound System; EVO XQ20 Diagnostic Ultrasound System; EVO XQ10 Diagnostic Ultrasound System; EVO QH30 Diagnostic Ultrasound System; EVO QH20 Diagnostic Ultrasound System; EVO QH10 Diagnostic Ultrasound System
K254099 is the FDA 510(k) clearance record for EVO Q30 Diagnostic Ultrasound System; EVO Q20 Diagnostic Ultrasound System; EVO Q10 Diagnostic Ultrasound System; EVO XQ30 Diagnostic Ultrasound System; EVO XQ20 Diagnostic Ultrasound System; EVO XQ10 Diagnostic Ultrasound System; EVO QH30 Diagnostic Ultrasound System; EVO QH20 Diagnostic Ultrasound System; EVO QH10 Diagnostic Ultrasound System, a class II device, cleared for Samsung Medison Co., Ltd. on under FDA product code IYN (System, Imaging, Pulsed Doppler, Ultrasonic). FDA records list 73 510(k) clearances for Samsung Medison Co., Ltd., from to . As of , FDA records show no recalls naming K254099.
Clearance record
- Decision date
- Received
- (98 days to decision)
- Product code
- IYN System, Imaging, Pulsed Doppler, Ultrasonic
- Regulation
- 21 CFR 892.1550
- Device class
- Class II
- Review panel
- Radiology
- Applicant
- Samsung Medison Co., Ltd. 3366, Hanseo-Ro, Nam-Myeon, Hongcheon-Gun, KR
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code IYN
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 6 |
| December 2025 | 6 |
| January 2026 | 4 |
| February 2026 | 1 |
| March 2026 | 6 |
| April 2026 | 3 |
| May 2026 | 11 |
| June 2026 | 3 |
| July 2026 | 6 |
| August 2026 | 3 |
| September 2026 | 3 |
| October 2026 | 0 |
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