Consona N9, Consona N9 Pro, Consona N9 Super, Consona Nova, Consona N9S, Consona NI, Consona NT, Nuewa N9, Recho N9, Consona N9 Exp, Consona N9 Elite, Resona N9, Consona N9T, Consona N8, Consona N8 Pro, Consona N8 Super, Consona OR, Consona N8S, Consona OI, Consona OT, Consona N8 Exp, Consona N8 Elite, Consona N8T, Consona N7, Consona N7 Pro, Consona N7 Super, Consona VR, Consona N7S, Consona VI, Consona VT, Consona N7 Exp, Consona N7 Elite, Consona N7T Diagnostic Ultrasound System
K221300 is the FDA 510(k) clearance record for Consona N9, Consona N9 Pro, Consona N9 Super, Consona Nova, Consona N9S, Consona NI, Consona NT, Nuewa N9, Recho N9, Consona N9 Exp, Consona N9 Elite, Resona N9, Consona N9T, Consona N8, Consona N8 Pro, Consona N8 Super, Consona OR, Consona N8S, Consona OI, Consona OT, Consona N8 Exp, Consona N8 Elite, Consona N8T, Consona N7, Consona N7 Pro, Consona N7 Super, Consona VR, Consona N7S, Consona VI, Consona VT, Consona N7 Exp, Consona N7 Elite, Consona N7T Diagnostic Ultrasound System, a class II device, cleared for Shenzhen Mindray Bio-Medical Electronics Co., Ltd. on under FDA product code IYN (System, Imaging, Pulsed Doppler, Ultrasonic). FDA records list 160 510(k) clearances for Shenzhen Mindray Bio-Medical Electronics Co., Ltd., from to . As of , FDA records show no recalls naming K221300.
Clearance record
- Decision date
- Received
- (147 days to decision)
- Product code
- IYN System, Imaging, Pulsed Doppler, Ultrasonic
- Regulation
- 21 CFR 892.1550
- Device class
- Class II
- Review panel
- Radiology
- Applicant
- Shenzhen Mindray Bio-Medical Electronics Co., Ltd. Keji 12th Rd. S., Hi-Tech Industrial Park, Shenzhen, CN
- 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 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
