Clearance Summary
21.3 5MP Color LCD Display UMD5-21B01 received FDA 510(k) clearance under submission number K241499, sponsored by Acula Technology Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2024-06-13.
- Submission: K241499
- Applicant / Sponsor: Acula Technology Corp.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2050
- Decision date: 2024-06-13
Classification & Regulation
This clearance is catalogued under FDA product code PGY and 21 CFR 892.2050, within the Radiology review panel as a Class II device.