Device Classification Name |
Lenses, Soft Contact, Daily Wear
More FDA Info for this Device |
510(K) Number |
K220143 |
Device Name |
Lenses, Soft Contact, Daily Wear |
Applicant |
Shenzhen Dashicheng Optical Technology Co., Ltd.
101, 201 and 301, Unit 3, Building 1
Wanjiening Industrial Park, No. 1450, Guanguang Road
Shenzhen 518110 CN
Other 510(k) Applications for this Company
|
Contact |
Jiayi Li
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 |
01/18/2022 |
Decision Date |
09/08/2022 |
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 |
|