K000571 is an FDA 510(k) clearance for the GE LOGIQ 700. This device is classified as a System, Imaging, Pulsed Echo, Ultrasonic (Class II - Special Controls, product code IYO).
Submitted by GE Medical Systems (Milwaukee, US). The FDA issued a Cleared decision on April 18, 2000, 56 days after receiving the submission on February 22, 2000.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1560.
| 510(k) Number | K000571 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 22, 2000 |
| Decision Date | April 18, 2000 |
| Days to Decision | 56 days |
| Submission Type | Special |
| 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 |