FDA 510(k) Application Details - K980039

Device Classification Name	Latex Patient Examination Glove   More FDA Info for this Device
510(K) Number	K980039
Device Name	Latex Patient Examination Glove
Applicant	SRI JOHANI SDN. BHD. LOT PT 7178, BALAKONG N/V, SERI KEMBANGAN SELANGOR 43300 MY Other 510(k) Applications for this Company
Contact	LIM L AIK 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	01/05/1998
Decision Date	02/09/1998
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