510(k) K061285

SMARTSITE NEEDLE FREE VALVE ADMINISTRATION SETS by Cardinal Health, Alaris Products — Product Code FPA

K061285 is an FDA 510(k) premarket notification submitted by Cardinal Health, Alaris Products for the device "SMARTSITE NEEDLE FREE VALVE ADMINISTRATION SETS". The FDA issued a decision of Substantially Equivalent on July 26, 2006. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Cardinal Health, Alaris Products has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 26, 2006
Date Received
May 8, 2006
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Set, Administration, Intravascular
Device Class
Class II
Regulation Number
880.5440
Review Panel
HO
Submission Type