Vlv Associates, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vlv Associates, Inc. - FDA 510(k) Cleared Devices
12
Total
11
Cleared
0
Denied
Vlv Associates, Inc. has 11 FDA 510(k) cleared general hospital devices. Based in East Hanover, US.
Historical record: 11 cleared submissions from 1986 to 1997.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vlv Associates, Inc.
12 devices
Cleared
Sep 29, 1997
SA-EF MULTI-LUMEN EXTENSION SET
General Hospital
49d
Cleared
Feb 28, 1997
SA.EF(TM) INFUSION PORT II - CONNECTOR AND EXTENSION SET
General Hospital
85d
Cleared
Feb 07, 1996
VLV SA.EF INFUSION PORT EXTENSION SETS
General Hospital
48d
Cleared
Oct 30, 1995
VLV SA EF INFUSION PORT
General Hospital
77d
Cleared
Jul 14, 1995
VLV SOLODRAW(TM) DUAL CHAMBER PISTON SYRINGE
General Hospital
242d
Cleared
Sep 02, 1994
DISPOSABLE, AMBULATORY, INFUSION PUMPS
General Hospital
218d
Cleared
Feb 15, 1994
PROMED BIOPSY NEEDLE
General & Plastic Surgery
221d
Cleared
Mar 15, 1993
PRO-LOK EXTENSION SET(S)
General Hospital
293d
Cleared
Oct 03, 1990
PRO-LOK (TM) EXTENSION SETS
General Hospital
21d
Cleared
Jun 08, 1990
VERSA-LOCK(TM) UNIVERSAL NEEDLE CONNECTOR
General Hospital
94d
Cleared
Jun 08, 1990
PRO-LOCK(TM) SHIELDING NEEDLE CONNECTOR ASSEMBLY
General Hospital
93d
Cleared
Jan 27, 1986
HOLD-IT FRAMED ADHESIVE FILM
General Hospital
21d