FDA 510(k) Application Details - K211103

Device Classification Name	Vinyl Patient Examination Glove   More FDA Info for this Device
510(K) Number	K211103
Device Name	Vinyl Patient Examination Glove
Applicant	Shanghai Shengda Medical Applications Co., Ltd No. 608 Xingwen Road, North Development Zone, Jiading District Shanghai 201815 CN Other 510(k) Applications for this Company
Contact	Ying Su Other 510(k) Applications for this Contact
Regulation Number	880.6250   More FDA Info for this Regulation Number
Classification Product Code	LYZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/13/2021
Decision Date	11/04/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review