FDA 510(k) Application Details - K251255

Device Classification Name	More FDA Info for this Device
510(K) Number	K251255
Device Name	LymphaTech Mobile 3D Measuring Tool
Applicant	Lymphatech, Inc. 976 Brady Ave NW Suite 100 Atlanta, GA 30318 US Other 510(k) Applications for this Company
Contact	Mike Weiler Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	SFG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/23/2025
Decision Date	07/22/2025
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review