510(k) K922115

IVAC NEEDLELESS INJECTION VALVE by Y — Product Code FPA

K922115 is an FDA 510(k) premarket notification submitted by Y for the device "IVAC NEEDLELESS INJECTION VALVE". The FDA issued a decision of Substantially Equivalent on October 12, 1993. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Y has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 12, 1993
Date Received
May 5, 1992
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