Becton Dickinson Vascular Access, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Becton Dickinson Vascular Access, Inc. - FDA 510(k) Cleared Devices
25
Total
22
Cleared
0
Denied
Becton Dickinson Vascular Access, Inc. has 22 FDA 510(k) cleared general hospital devices. Based in Sandy, US.
Historical record: 22 cleared submissions from 1992 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 - Becton Dickinson Vascular Access, Inc.
25 devices
Cleared
Dec 24, 1997
INSYTE, INSYTE-W, INSYTE AUTOGUARD CATHETERS
General Hospital
258d
Cleared
Apr 08, 1997
E-Z SET INFUSION SET/SAF-T E-Z SET INFUSION SET
General Hospital
75d
Cleared
Jan 06, 1997
FIRST MIDCATH CATHETER KIT
General Hospital
89d
Cleared
Jan 06, 1997
FIRST MIDCATH CATHETER WITH DUAL LUMENS
General Hospital
89d
Cleared
Jan 06, 1997
FIRST MIDCATH CATHETER
General Hospital
89d
Cleared
Apr 08, 1996
FIRST PICC INTRODUCER CATHETER
Cardiovascular
166d
Cleared
Jul 31, 1995
ANGIOCATH, NOVBALON, ANGIO-SET INTRAVASCULAR & ANGIOCATH INTRODUCTION...
General Hospital
45d
Cleared
Jul 31, 1995
ANGIOCATH & INSYTE AUTOGUARD CATHETERS
General Hospital
39d
Cleared
May 31, 1995
E-Z SET, SAF-T E-Z SET, AND MINICATH INFUSION SETS
General Hospital
30d
Cleared
Apr 18, 1995
ANGIOCATH(R) NONVALON(R) AND ANGIO-SET(R) IV CATHETERS
General Hospital
83d
Cleared
Mar 15, 1995
SAFEDWEEL DRESSING CHANGE TRAY
General Hospital
41d
Cleared
Mar 14, 1995
DESERET(R) I.V. LOOP AND DESERET (R) J LOOP
General Hospital
48d