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FDA 510(k) Application Details - K242533
Device Classification Name
Polymer Patient Examination Glove
More FDA Info for this Device
510(K) Number
K242533
Device Name
Polymer Patient Examination Glove
Applicant
Better Care Plastic Technology Co., Ltd.
Fuqian Xi Road, West district of Shenze Industrial Base
Shenze County 050000 CN
Other 510(k) Applications for this Company
Contact
Chunyan Zhu
Other 510(k) Applications for this Contact
Regulation Number
880.6250
More FDA Info for this Regulation Number
Classification Product Code
LZA
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/26/2024
Decision Date
03/18/2025
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
FDA Source Information for K242533
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