FDA 510(k) Application Details - K013996

Device Classification Name	Latex Patient Examination Glove   More FDA Info for this Device
510(K) Number	K013996
Device Name	Latex Patient Examination Glove
Applicant	PT. MAJA AGUNG LATEXINDO 5445 DANIEL ST. CHINO, CA 91710 US Other 510(k) Applications for this Company
Contact	EMMY T JOENG 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	12/03/2001
Decision Date	02/26/2002
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