510(k) K901046

VERSA-LOCK(TM) UNIVERSAL NEEDLE CONNECTOR by Vlv Associates, Inc. — Product Code FPA

K901046 is an FDA 510(k) premarket notification submitted by Vlv Associates, Inc. for the device "VERSA-LOCK(TM) UNIVERSAL NEEDLE CONNECTOR". The FDA issued a decision of Substantially Equivalent on June 8, 1990. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Vlv Associates, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 8, 1990
Date Received
March 6, 1990
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