510(k) K060580

K-SHIELD PORT ACCESS INFUSION SET by Kawasumi Laboratories, Inc. — Product Code FPA

K060580 is an FDA 510(k) premarket notification submitted by Kawasumi Laboratories, Inc. for the device "K-SHIELD PORT ACCESS INFUSION SET". The FDA issued a decision of Substantially Equivalent on June 6, 2006. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Kawasumi Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 6, 2006
Date Received
March 6, 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