Nihon Kohden America, Inc. · Class II · Cleared Sep 3, 1992
| K-number | K920743 |
| Device name | DUAL LEAD (ECG1 & ECG2) ARRHYTHMIA ANALYSIS |
| Applicant | Nihon Kohden America, Inc. |
| Product code | DSI |
| Device class | Class II |
| Decision date | Sep 3, 1992 |
| Decision | Substantially Equivalent |
| Regulation | 870.1025 |
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