Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Display, Diagnostic Radiology
510(k) Number K261213
Device Name Medical Monitor (40HT513D)
Applicant
Lg Electronics.Inc
168, Suchul-Daero
Gumi-Si,  KR 39368
Applicant Contact Wonhi Lee
Correspondent
Lg Electronics.Inc
168, Suchul-Daero
Gumi-Si,  KR 39368
Correspondent Contact Wonhi Lee
Regulation Number892.2050
Classification Product Code
PGY  
Date Received04/14/2026
Decision Date 06/12/2026
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-