K080760Substantially Equivalent
Acuson X300 Ultrasound System
Siemens Medical Solutions USA, Inc., Ultrasound di, Mountainview CA / Special, Substantially Equivalent
K080760 is the FDA 510(k) clearance record for ACUSON X300 ULTRASOUND SYSTEM, a class II device, cleared for Siemens Medical Solutions USA, Inc., Ultrasound DI on under FDA product code IYN (System, Imaging, Pulsed Doppler, Ultrasonic). FDA records list 11 510(k) clearances for Siemens Medical Solutions USA, Inc., Ultrasound DI, from to . As of , FDA records show no recalls naming K080760.
Clearance record
- Decision date
- Received
- (38 days to decision)
- Product code
- IYN System, Imaging, Pulsed Doppler, Ultrasonic
- Regulation
- 21 CFR 892.1550
- Device class
- Class II
- Review panel
- Radiology
- Applicant
- Siemens Medical Solutions USA, Inc., Ultrasound DI 1230 Shorebird Way, Mountainview CA
- 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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