FDA 510(k) Application Details - K203593

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K203593
Device Name	Polymer Patient Examination Glove
Applicant	Guang Dong Kingfa SCI. & TECH.CO., LTD. No. 28 Delong Ave., Shijiao Town, Qingcheng District Qingyuan 511545 CN Other 510(k) Applications for this Company
Contact	Xiaoge Yu 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	12/09/2020
Decision Date	03/19/2021
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