FDA 510(k) Application Details - K240130

Device Classification Name	More FDA Info for this Device
510(K) Number	K240130
Device Name	Medical Monitor (21HQ613D)
Applicant	LG Electronics Inc. 168, Suchul-Daero Gumi-Si 39368 KR Other 510(k) Applications for this Company
Contact	Hanseul Park Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	PGY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/17/2024
Decision Date	02/15/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review