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FDA 510(k) Application Details - K232716
Device Classification Name
Powered Laser Surgical Instrument
More FDA Info for this Device
510(K) Number
K232716
Device Name
Powered Laser Surgical Instrument
Applicant
Hebei Zhemai Technology Co., Ltd
1st FL, N of No.1 Warehouse, W of Shuichang Rd, N of Beiyi
Rd, Yanjiao Development Zone, Sanhe
Langfang 065201 CN
Other 510(k) Applications for this Company
Contact
Yuting Qu
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
09/05/2023
Decision Date
11/30/2023
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 K232716
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