FDA 510(k) Application Details - K091736

Device Classification Name	Container, Sharps   More FDA Info for this Device
510(K) Number	K091736
Device Name	Container, Sharps
Applicant	DANIELS CORPORATION PTY, INC. 2133-126 UPTON DRIVE SUITE 436 VIRGINIA BEACH, VA 23454 US Other 510(k) Applications for this Company
Contact	ANDREA ARREDONDO Other 510(k) Applications for this Contact
Regulation Number	880.5570   More FDA Info for this Regulation Number
Classification Product Code	MMK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/11/2009
Decision Date	10/30/2009
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