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Lg ASHK100G

by LG Electronics Inc. 3 variants

Lg ASHK100G is a Class II device made by LG Electronics Inc., listed in FDA GUDID since 5 Sep 2019 (UDI-DI 00719192635272), registry data as of 12 Nov 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00719192635272 UDI-DI Date5 Sep 2019ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Lg
Generic name
Diagnostic x-ray digital imaging system workstation application software
Model / reference
ASHK100G
Primary DI / UDI-DI
00719192635272
FDA product code
LLZ
GMDN term
Diagnostic x-ray digital imaging system workstation application software
Device class
Class II
Regulation number
892.2050
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LLZ (System, Image Processing, Radiological).

Other devices from LG Electronics Inc.

See all devices from LG Electronics Inc. →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)