Nihon Kohden America, Inc. · Class II · Cleared Feb 12, 1982
| K-number | K820067 |
| Device name | ELECTROENCEPHALOGRAPH ECG-6151 |
| Applicant | Nihon Kohden America, Inc. |
| Product code | DPS |
| Device class | Class II |
| Decision date | Feb 12, 1982 |
| Decision | Substantially Equivalent |
| Regulation | 870.2340 |
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