Nihon Kohden America, Inc. · Class II · Cleared Jul 9, 1997
| K-number | K971194 |
| Device name | NIHON KOHDEN TEC-6100A CARDIOLIFE MINI DEFIBRILLATOR & ACCESSORIES |
| Applicant | Nihon Kohden America, Inc. |
| Product code | LDD |
| Device class | Class II |
| Decision date | Jul 9, 1997 |
| Decision | Substantially Equivalent - Subject to Tracking Reg. |
| Regulation | 870.5300 |
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