FDA 510(k) Application Details - K982440

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K982440
Device Name	Polymer Patient Examination Glove
Applicant	PERUSAHAAN GETAH ASAS SDN BHD LOT 754, JALAN HAJI SIRAT OFF JALAN KAPAR, KLANG SELANGOR, DARUL EHSAN 42100 MY Other 510(k) Applications for this Company
Contact	BOB CHAN 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	07/14/1998
Decision Date	09/30/1998
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