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FDA 510(k) Application Details - K241881
Device Classification Name
Light Based Over-The-Counter Hair Removal
More FDA Info for this Device
510(K) Number
K241881
Device Name
Light Based Over-The-Counter Hair Removal
Applicant
SHENZHEN JUNMEI TECHNOLOGY CO., LTD.
Plant 4301, Yili Science Park, No.596-4, Dahe Village,
Guancheng Community, Guanhu Street, Longhua District
Shenzhen 518000 CN
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Contact
Zenghui Guo
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
06/28/2024
Decision Date
08/29/2024
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
FDA Source Information for K241881
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