FDA 510(k) Application Details - K022343

Device Classification Name	Latex Patient Examination Glove   More FDA Info for this Device
510(K) Number	K022343
Device Name	Latex Patient Examination Glove
Applicant	PT. WRP BUANA MULTICORPORA JALAN JERMAL #20B, KELURAHAN SEI MATI, MEDAN LABUHAN KM 17 MEDAN 20252 ID Other 510(k) Applications for this Company
Contact	NG POY SIN 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	07/19/2002
Decision Date	09/16/2002
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