FDA 510(k) Application Details - K022368

Device Classification Name	Vinyl Patient Examination Glove   More FDA Info for this Device
510(K) Number	K022368
Device Name	Vinyl Patient Examination Glove
Applicant	CANOPUS MEDICAL SUPPLY CO., LTD. 10TH FL.,NO. 201 FU HSING NORTH ROAD TAIPEI 105 TW Other 510(k) Applications for this Company
Contact	RUBY LIN Other 510(k) Applications for this Contact
Regulation Number	880.6250   More FDA Info for this Regulation Number
Classification Product Code	LYZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/22/2002
Decision Date	09/05/2002
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