SCW
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Digital Prismatic Correction
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 886.1655
- Medical specialty
- Ophthalmic
- FDA definition
- The device is intended to provide digital image adjustments in a display system in accordance with a users prism prescription. The device can be used in conjunction with optical lenses for refractive correction.
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| Record | Firm | Date |
|---|---|---|
| Digital Prism Correction Feature (DPCF) (K250143) | Apple, Inc. | 2025-06-23 |
| Digital Prism Correction Feature (DPCF) (K242058) | Apple, Inc. | 2024-10-21 |
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