FDA 510(k) Applications Submitted by Rajitha Nair
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K223508 | 11/22/2022 | Cardioblate Gemini-s 49260 Surgical Ablation Device; Cardioblate Gemini-s 49351 Surgical Ablation Device | Medtronic Inc. |
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