K031927 is an FDA 510(k) clearance for the GE DELTA SOFTWARE OPTION FOR MRI. This device is classified as a System, Nuclear Magnetic Resonance Imaging (Class II - Special Controls, product code LNH).
Submitted by GE Medical Systems (Waukesha, US). The FDA issued a Cleared decision on July 2, 2003, 9 days after receiving the submission on June 23, 2003.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1000.
| 510(k) Number | K031927 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 23, 2003 |
| Decision Date | July 02, 2003 |
| Days to Decision | 9 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | LNH - System, Nuclear Magnetic Resonance Imaging |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1000 |