| Document Number | 2024-06037 |
| Type | Proposed Rule |
| Published | Mar 26, 2024 |
| Effective Date | - |
| RIN | 0910-AI84 |
| Docket ID | Docket No. FDA-2023-N-3902 |
| Text Fetched | No |
| Part | Name | Agency |
|---|---|---|
| 21 CFR 882 | Neurological Devices... | - |
| 21 CFR 895 | Banned Devices... | - |
| Type | Proposed | Final | Method | Conf |
|---|---|---|---|---|
| No paired documents | ||||
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