K970901 is an FDA 510(k) clearance for the GE LOGIQ 500 DIAGNOSTIC ULTRASOUND SYSTEM. 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 December 22, 1997, 286 days after receiving the submission on March 11, 1997.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1560.
| 510(k) Number | K970901 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 11, 1997 |
| Decision Date | December 22, 1997 |
| Days to Decision | 286 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 |