FDA 510(k) Application Details - K121368

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K121368
Device Name	Polymer Patient Examination Glove
Applicant	MATANG MFG. SDN. BHD. LOT 10, KAWASAN PERINDUSTRIAN SERKAM, MUKIM SERKAM MERLIMAU, MELAKA 77300 MY Other 510(k) Applications for this Company
Contact	LESLIE LEONG 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	05/07/2012
Decision Date	08/10/2012
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