Medtronic, Inc. · Class II · Cleared Dec 22, 2022
| K-number | K223508 |
| Device name | Cardioblate Gemini-s 49260 Surgical Ablation Device; Cardioblate Gemini-s 49351 Surgical Ablation Device |
| Applicant | Medtronic, Inc. |
| Product code | OCL |
| Device class | Class II |
| Decision date | Dec 22, 2022 |
| Decision | Substantially Equivalent |
| Regulation | 878.4400 |
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