FDA 510(k) Application Details - K241884

Device Classification Name	Lenses, Soft Contact, Daily Wear   More FDA Info for this Device
510(K) Number	K241884
Device Name	Lenses, Soft Contact, Daily Wear
Applicant	Hunan Haipuming Technology Co., Ltd. The Intersection of Chuangye Avenue and Lvting Avenue Dahetang Sub-district Office, Shaodong City Shaoyang 422800 CN Other 510(k) Applications for this Company
Contact	Mingxuan Zhang Other 510(k) Applications for this Contact
Regulation Number	886.5925   More FDA Info for this Regulation Number
Classification Product Code	LPL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/28/2024
Decision Date	03/20/2025
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review