Fukuda Denshi USA, Inc. · Class II · Cleared Nov 14, 1985
| K-number | K853352 |
| Device name | FUKUDA DENSHI DS-1060 DYNASCOPE PATIENT MONITOR |
| Applicant | Fukuda Denshi USA, Inc. |
| Product code | DSI |
| Device class | Class II |
| Decision date | Nov 14, 1985 |
| Decision | Substantially Equivalent |
| Regulation | 870.1025 |
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