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FDA 510(k) Application Details - K241547
Device Classification Name
Powered Laser Surgical Instrument
More FDA Info for this Device
510(K) Number
K241547
Device Name
Powered Laser Surgical Instrument
Applicant
WeiFang Dragonfly Electronics Technology Co., Ltd
Southásideáofátheásecondáfloor,áProduction workshop
No.1, No.á13426áYuqingáEast Street,áWeifangáHigh-techáZone
Weifang 261061 CN
Other 510(k) Applications for this Company
Contact
Ray Zhao
Other 510(k) Applications for this Contact
Regulation Number
878.4810
More FDA Info for this Regulation Number
Classification Product Code
GEX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
05/31/2024
Decision Date
08/13/2024
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 K241547
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