FDA device listing

19HK312C, 27HJ712C, 27HJ713C, 27HS713C,24CK560N,24CN670NK, 24CN670WK, 24CN670IK,24CR670NK, 24CR670WK, 24CR670IK…

FDA device listing 1907878090 · LG Electronics Inc Monitor Division.

Key facts

Proprietary names 19HK312C, 27HJ712C, 27HJ713C, 27HS713C,24CK560N,24CN670NK, 24CN670WK, 24CN670IK,24CR670NK, 24CR670WK, 24CR670IK, 24CR671NK, 24CR671WK, 24CR671IK, 24CR670W,27HJ710S, 27HK510S, 27HQ710S, 32HL710S, 32HL714S, 55MH5K, AR-3250-3212,32HST70S,MLW-2750UHD
Owner/operator LG Electronics Inc Monitor Division.
Owner/operator number 10053135
Product codes FWB
Device names FWB - Camera, Television, Surgical, Without Audio
Device class Class I
Classification regulations (21 CFR) 878.4160
Review panels General & Plastic Surgery
Registered establishments LG ELECTRONICS INC., LG Electronics Nanjing New Technology Co., Ltd.
Establishment registrations 3004434200, 3013501671
FEI numbers 3004434200, 3013501671
Establishment operations Foreign Exporter, Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None listed Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

Browse all FDA device listings