FDA 510(k) Application Details - K220222

Device Classification Name Light Based Over-The-Counter Hair Removal

  More FDA Info for this Device
510(K) Number K220222
Device Name Light Based Over-The-Counter Hair Removal
Applicant Shenzhen Yuwei Electronic Technology Co., Ltd.
409, Building 3, 1970 Science Park, Minzhi Community
Minzhi Street, Longhua District
Shenzhen 518000 CN
Other 510(k) Applications for this Company
Contact Liu Xuemeng
Other 510(k) Applications for this Contact
Regulation Number 878.4810

  More FDA Info for this Regulation Number
Classification Product Code OHT
Other 510(k) Applications for this Device

  More FDA Info for this Product Code
Date Received 01/26/2022
Decision Date 04/26/2022
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



Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact