Vlv Associates, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
6
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K972957SA-EF MULTI-LUMEN EXTENSION SETSeptember 29, 1997
K964876SA.EF(TM) INFUSION PORT II - CONNECTOR AND EXTENSION SETFebruary 28, 1997
K955783VLV SA.EF INFUSION PORT EXTENSION SETSFebruary 7, 1996
K953791VLV SA EF INFUSION PORTOctober 30, 1995
K945592VLV SOLODRAW(TM) DUAL CHAMBER PISTON SYRINGEJuly 14, 1995
K940406DISPOSABLE, AMBULATORY, INFUSION PUMPSSeptember 2, 1994
K933364PROMED BIOPSY NEEDLEFebruary 15, 1994
K922469PRO-LOK EXTENSION SET(S)March 15, 1993
K904217PRO-LOK (TM) EXTENSION SETSOctober 3, 1990
K901081PRO-LOCK(TM) SHIELDING NEEDLE CONNECTOR ASSEMBLYJune 8, 1990
K901046VERSA-LOCK(TM) UNIVERSAL NEEDLE CONNECTORJune 8, 1990
K860071HOLD-IT FRAMED ADHESIVE FILMJanuary 27, 1986