FDA 510(k) Application Details - K243133

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K243133
Device Name	Polymer Patient Examination Glove
Applicant	KL-Kepong Rubber Products SDN. BHD. Lot 134905, ╛ Mile Off Jalan Bercham Kawasan Perindustrian Bercham Ipoh 31400 MY Other 510(k) Applications for this Company
Contact	Phooi Yann Cheng 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	09/30/2024
Decision Date	06/17/2025
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