FDA 510(k) Application Details - K033229

Device Classification Name	Vinyl Patient Examination Glove   More FDA Info for this Device
510(K) Number	K033229
Device Name	Vinyl Patient Examination Glove
Applicant	BERNARD TECHNOLOGIES, INC. 75 EAST WACKER DRIVE CHICAGO, IL 60601 US Other 510(k) Applications for this Company
Contact	MICHAEL D LELAH, PHD 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	10/06/2003
Decision Date	12/17/2003
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