Ge Medical Systems Information Technologies · Class II · Cleared Feb 1, 2002
| K-number | K020022 |
| Device name | DINAMAP PRO SERIES MONITOR, MODELS 110, 210, 310, 410 |
| Applicant | Ge Medical Systems Information Technologies |
| Product code | MWI |
| Device class | Class II |
| Decision date | Feb 1, 2002 |
| Decision | Substantially Equivalent |
| Regulation | 870.2300 |
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