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Beacon

FDA UDI

Class II (US FDA UDI)

by Shenzhen Beacon Display Technology Co., Ltd.

Identity

Trade Name
Beacon FDA UDI
Generic Name
Pathology information system FDA UDI
Device Name
8MP Color LCD Display FDA UDI
Model / Reference
PA27 FDA UDI
Description
8MP Color LCD Display FDA UDI

Identifiers

Primary DI / UDI-DI
06970027821084 FDA UDI
510(k) Number
K233119 FDA UDI
FDA Product Code
PZZ FDA UDI
GMDN Term
Pathology information system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.3700 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Pathology information system

Beacon by Shenzhen Beacon Display Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pathology information system.

Cleared under the same submission

K233119 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Shenzhen Beacon Display Technology Co., Ltd.

Sources (1)

  • FDA UDI 182f5dba-6994-46cf-8826-3cf43cc682ad 34 fields · synced May 30, 2026