510(k) K082362

SURSHIELD SAFETY I.V. CATHETER by Terumo Medical Corp. — Product Code FOZ

K082362 is an FDA 510(k) premarket notification submitted by Terumo Medical Corp. for the device "SURSHIELD SAFETY I.V. CATHETER". The FDA issued a decision of Substantially Equivalent on September 17, 2008. The device falls under product code FOZ (Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days), a Class II device regulated under 21 CFR 880.5200. Terumo Medical Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 17, 2008
Date Received
August 18, 2008
Clearance Type
Traditional
Expedited Review
No
Third Party Review
Yes

Device Classification

Device Name
Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Device Class
Class II
Regulation Number
880.5200
Review Panel
HO
Submission Type