510(k) K071108

TEXIUM SYRINGE by Cardinal Health, Alaris Products — Product Code FMF

K071108 is an FDA 510(k) premarket notification submitted by Cardinal Health, Alaris Products for the device "TEXIUM SYRINGE". The FDA issued a decision of Substantially Equivalent on May 24, 2007. The device falls under product code FMF (Syringe, Piston), a Class II device regulated under 21 CFR 880.5860. Cardinal Health, Alaris Products has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 24, 2007
Date Received
April 19, 2007
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Syringe, Piston
Device Class
Class II
Regulation Number
880.5860
Review Panel
HO
Submission Type