FDA 510(k) Application Details - K242500

Device Classification Name	More FDA Info for this Device
510(K) Number	K242500
Device Name	LARALAB
Applicant	LARALAB GmbH Herzog-Heinrich-Str.13, 80336 Munich DE Other 510(k) Applications for this Company
Contact	Julian Bernard Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QIH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/22/2024
Decision Date	04/16/2025
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review