Ge Medical Systems Information Technologies · Class II · Cleared May 22, 2002
| K-number | K021435 |
| Device name | DINAMAP PRO SERIES MONITOR, MODELS 110N,210N,310N,410N |
| Applicant | Ge Medical Systems Information Technologies |
| Product code | MWI |
| Device class | Class II |
| Decision date | May 22, 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