Beacon PA27
by Shenzhen Beacon Display Technology Co., Ltd.
Beacon PA27 is a Class II device made by Shenzhen Beacon Display Technology Co., Ltd., cleared under FDA 510(k) K233119 on 28 Dec 2024 and listed in FDA GUDID since 18 Mar 2025 (UDI-DI 06970027821084), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number06970027821084 | Date18 Mar 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK233119 | Date28 Dec 2024 | StatusActive |
Official records
- AccessGUDID record 06970027821084
- FDA 510(k) database K233119
Across registries
- FDA 510(k) K233119 decided 28 Dec 2024 Active
- FDA GUDID UDI-DI 06970027821084 listed 18 Mar 2025 Listed
Timeline
- Cleared FDA 510(k) K233119
- Listed FDA GUDID 06970027821084
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Beacon
- Generic name
- Pathology information system
- Model / reference
- PA27
- Primary DI / UDI-DI
- 06970027821084
- 510(k) Number
- FDA product code
- PZZ
- GMDN term
- Pathology information system
- Device class
- Class II
- Regulation number
- 864.3700
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
Similar devices
Other devices filed under FDA product code PZZ (Digital Pathology Display).
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