Ge Medical Systems, LLC · Class II · Cleared Jun 9, 2016
| K-number | K160618 |
| Device name | Discovery MR750 3.0T, Discovery MR450 1.5T, Discovery MR750w 3.0T, Optima MR450w 1.5T |
| Applicant | Ge Medical Systems, LLC |
| Product code | LNH |
| Device class | Class II |
| Decision date | Jun 9, 2016 |
| Decision | Substantially Equivalent |
| Regulation | 892.1000 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov