K143368 is an FDA 510(k) clearance for the GenIQ. This device is classified as a System, Image Processing, Radiological (Class II - Special Controls, product code LLZ).
Submitted by Ge Medical Systems, LLC (Waukesha, US). The FDA issued a Cleared decision on July 29, 2015, 246 days after receiving the submission on November 25, 2014.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.2050.
| 510(k) Number | K143368 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 25, 2014 |
| Decision Date | July 29, 2015 |
| Days to Decision | 246 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | LLZ — System, Image Processing, Radiological |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.2050 |