FDA 510(k) Application Details - K241970

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K241970
Device Name	Polymer Patient Examination Glove
Applicant	Kanglongda Vietnam Protection Technology Company Limited Lot CN 05, Viglacera-Phong Dien Industrial Park, Phong Hoa Commune, Phong Dien District Thua Thien Hue 49316 VN Other 510(k) Applications for this Company
Contact	Yao Yuxiang 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	07/05/2024
Decision Date	08/02/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review