FDA 510(k) Application Details - K010572

Device Classification Name	Drape, Surgical   More FDA Info for this Device
510(K) Number	K010572
Device Name	Drape, Surgical
Applicant	BECTON DICKINSON AND CO. 7575 COMMERCE COURT SARASOTA, FL 34243-3212 US Other 510(k) Applications for this Company
Contact	JAMES STAFFIERA Other 510(k) Applications for this Contact
Regulation Number	878.4370   More FDA Info for this Regulation Number
Classification Product Code	KKX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/26/2001
Decision Date	03/12/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review