K071314 is an FDA 510(k) clearance for the SONOLINE G20 DIAGNOSTIC ULTRASOUND SYSTEMS. This device is classified as a System, Imaging, Pulsed Echo, Ultrasonic (Class II - Special Controls, product code IYO).
Submitted by Siemens Medical Solutions USA, Inc. (Mountainview, US). The FDA issued a Cleared decision on May 22, 2007, 12 days after receiving the submission on May 10, 2007.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1560.
| 510(k) Number | K071314 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 10, 2007 |
| Decision Date | May 22, 2007 |
| Days to Decision | 12 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | IYO — System, Imaging, Pulsed Echo, Ultrasonic |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1560 |