510(k) K011405

EXEL INJECTION PLUG WITH CAP by Exelint Intl. Co. — Product Code FPA

K011405 is an FDA 510(k) premarket notification submitted by Exelint Intl. Co. for the device "EXEL INJECTION PLUG WITH CAP". The FDA issued a decision of Substantially Equivalent on September 27, 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
September 27, 2001
Date Received
May 8, 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