FDA 510(k) Application Details - K173053

Device Classification Name	Latex Patient Examination Glove   More FDA Info for this Device
510(K) Number	K173053
Device Name	Latex Patient Examination Glove
Applicant	Professional Latex Sdn Bhd Lot 52, Jalan Logam 2, Kamunting Raya lndustrial Kamunting 34600 MY Other 510(k) Applications for this Company
Contact	Yoon Lim Kok Other 510(k) Applications for this Contact
Regulation Number	880.6250   More FDA Info for this Regulation Number
Classification Product Code	LYY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/28/2017
Decision Date	06/06/2018
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