FDA 510(k) Application Details - K241750

Device Classification Name	Lancet, Blood   More FDA Info for this Device
510(K) Number	K241750
Device Name	Lancet, Blood
Applicant	Medifun Corporation 4F-1, 4F-9, 4F-10, No.99, Jingke S. Rd., Nantun Dist., Taichung City 408 TW Other 510(k) Applications for this Company
Contact	Aaron Chen Other 510(k) Applications for this Contact
Regulation Number	878.4800   More FDA Info for this Regulation Number
Classification Product Code	FMK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/18/2024
Decision Date	08/15/2024
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