FDA 510(k) Application Details - K051655

Device Classification Name	Cannula, Catheter   More FDA Info for this Device
510(K) Number	K051655
Device Name	Cannula, Catheter
Applicant	ANGIODYNAMICS, INC. 603 QUEENSBURY AVE. QUEENSBURY, NY 12804 US Other 510(k) Applications for this Company
Contact	TERI JUCKETT Other 510(k) Applications for this Contact
Regulation Number	870.1300   More FDA Info for this Regulation Number
Classification Product Code	DQR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/21/2005
Decision Date	09/12/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review