510(k) K072894

SURFLO WINGED INFUSION SET WITH NEEDLE PROTECTION (SURSHIELD) by Terumo Europe N.V. — Product Code FPA

K072894 is an FDA 510(k) premarket notification submitted by Terumo Europe N.V. for the device "SURFLO WINGED INFUSION SET WITH NEEDLE PROTECTION (SURSHIELD)". The FDA issued a decision of Substantially Equivalent on November 6, 2007. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Terumo Europe N.V. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 6, 2007
Date Received
October 11, 2007
Clearance Type
Special
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