510(k) K010404

EXEL I.V. ADMINISTRATION SET by Exelint Intl. Co. — Product Code FPA

K010404 is an FDA 510(k) premarket notification submitted by Exelint Intl. Co. for the device "EXEL I.V. ADMINISTRATION SET". The FDA issued a decision of Substantially Equivalent on August 30, 2001. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Exelint Intl. Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 30, 2001
Date Received
February 12, 2001
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