Nihon Kohden America, Inc. · Class II · Cleared Aug 2, 1988
| K-number | K880575 |
| Device name | CARDIOLIFE TEC-7300 W/OPTIONAL ACCESSORIES |
| Applicant | Nihon Kohden America, Inc. |
| Product code | LDD |
| Device class | Class II |
| Decision date | Aug 2, 1988 |
| Decision | Substantially Equivalent |
| Regulation | 870.5300 |
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