FDA 510(k) Application Details - K183068

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K183068
Device Name	Polymer Patient Examination Glove
Applicant	Haining Medical Products Co., Ltd. West of Dianchang Road, Luannan County Tangshan 063500 CN Other 510(k) Applications for this Company
Contact	Zhiming Yao 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	11/05/2018
Decision Date	12/21/2018
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