Becton Dickinson Vascular Access, Inc.
Sandy, UT, US
Becton Dickinson Vascular Access, Inc. appears in FDA device records in Sandy, UT. FDA records list 25 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 25
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 25 510(k) clearances for Becton Dickinson Vascular Access, Inc. between 1992 and 1997. The busiest year on record is 1995, with 12. The most recent is 1997, with 5.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1992 | 3 |
| 1993 | 2 |
| 1994 | 2 |
| 1995 | 12 |
| 1996 | 1 |
| 1997 | 5 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K971339 | INSYTE, INSYTE-W, INSYTE AUTOGUARD CATHETERS | FOZ | Substantially Equivalent | |
| K970259 | E-Z SET INFUSION SET/SAF-T E-Z SET INFUSION SET | FPA | Substantially Equivalent | |
| K964050 | FIRST MIDCATH CATHETER | FOZ | Substantially Equivalent | |
| K964049 | FIRST MIDCATH CATHETER WITH DUAL LUMENS | FOZ | Substantially Equivalent | |
| K964048 | FIRST MIDCATH CATHETER KIT | FOZ | Substantially Equivalent | |
| K954906 | FIRST PICC INTRODUCER CATHETER | DYB | Substantially Equivalent | |
| K952861 | ANGIOCATH & INSYTE AUTOGUARD CATHETERS | FOZ | Substantially Equivalent | |
| K952757 | ANGIOCATH, NOVBALON, ANGIO-SET INTRAVASCULAR & ANGIOCATH INTRODUCTION DRAINAGE CATHETER | FOZ | Substantially Equivalent | |
| K952053 | E-Z SET, SAF-T E-Z SET, AND MINICATH INFUSION SETS | FPA | Substantially Equivalent | |
| K950301 | ANGIOCATH(R) NONVALON(R) AND ANGIO-SET(R) IV CATHETERS | FOZ | Substantially Equivalent | |
| K950438 | SAFEDWEEL DRESSING CHANGE TRAY | FRG | Unknown | |
| K950439 | INSYTE SIDEHOLDED DRAINAGE CATHETER | GBX | Substantially Equivalent | |
| K950437 | ANGIOCATH SIDEHOLDER DRAINAGE CATHETER | GBX | Substantially Equivalent | |
| K950304 | DESERET (R) T-PORT (R) MULTI FLO(TM) AND DESERET (R)PRN ADAPTER | FPA | Substantially Equivalent | |
| K950303 | DESERET(R) I.V. LOOP AND DESERET (R) J LOOP | FPA | Substantially Equivalent | |
| K950302 | E-Z SET(R) AND MINICATH(R) INFUSION SETS | FPA | Substantially Equivalent | |
| K942045 | INSYTE INTRODUCER CATHETER | FOZ | Substantially Equivalent | |
| K941429 | IV CATHETER AND OBTURATOR | FOS | Substantially Equivalent | |
| K943941 | SAFESTART VASCULAR ACCESS START KIT | LRS | Substantially Equivalent | |
| K941283 | INNERSENSE DISPOSABLE MICROTRANSDUCER | DXO | Substantially Equivalent | |
| K923702 | INTIMA POINT GUARD INTRAVASCULAR CATHETER | FOZ | Substantially Equivalent | |
| K924737 | INNERSENSE(TM) DISPOSABLE MICROTRANSDUCER | DXO | Substantially Equivalent | |
| K921845 | INSYTE ARTCATH ARTERIAL CATHETERIZATION UNIT | DQO | Substantially Equivalent | |
| K914528 | SAFEDWEL(R) CENTRAL VENOUS CATHETER | FOZ | Unknown | |
| K914180 | DESERET(R) FLOW RESTRICTION VALVE | FOZ | Unknown |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain