| K-number | K123068 |
| Device name | OPTIMA MR 430S |
| Applicant | Ge Medical Systems, LLC |
| Product code | LNH |
| Device class | Class II |
| Decision date | Nov 13, 2012 |
| 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