Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Becton Dickinson Vascular Access, Inc. — Predicate Candidate Screening

25 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

83 daysmedian FDA review time
335 days90th percentile
25clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K971339INSYTE, INSYTE-W, INSYTE AUTOGUARD CATHETERSBecton Dickinson Vascular Access, Inc.1997-12-242580
K970259E-Z SET INFUSION SET/SAF-T E-Z SET INFUSION SETBecton Dickinson Vascular Access, Inc.1997-04-08750
K964050FIRST MIDCATH CATHETERBecton Dickinson Vascular Access, Inc.1997-01-06890
K964048FIRST MIDCATH CATHETER KITBecton Dickinson Vascular Access, Inc.1997-01-06890
K964049FIRST MIDCATH CATHETER WITH DUAL LUMENSBecton Dickinson Vascular Access, Inc.1997-01-06890
K954906FIRST PICC INTRODUCER CATHETERBecton Dickinson Vascular Access, Inc.1996-04-081660
K952757ANGIOCATH, NOVBALON, ANGIO-SET INTRAVASCULAR & ANGIOCATH INTBecton Dickinson Vascular Access, Inc.1995-07-31450
K952861ANGIOCATH & INSYTE AUTOGUARD CATHETERSBecton Dickinson Vascular Access, Inc.1995-07-31390
K952053E-Z SET, SAF-T E-Z SET, AND MINICATH INFUSION SETSBecton Dickinson Vascular Access, Inc.1995-05-31300
K950301ANGIOCATH(R) NONVALON(R) AND ANGIO-SET(R) IV CATHETERSBecton Dickinson Vascular Access, Inc.1995-04-18830
K950438SAFEDWEEL DRESSING CHANGE TRAYBecton Dickinson Vascular Access, Inc.1995-03-15410
K950437ANGIOCATH SIDEHOLDER DRAINAGE CATHETERBecton Dickinson Vascular Access, Inc.1995-03-14400
K950303DESERET(R) I.V. LOOP AND DESERET (R) J LOOPBecton Dickinson Vascular Access, Inc.1995-03-14480
K950439INSYTE SIDEHOLDED DRAINAGE CATHETERBecton Dickinson Vascular Access, Inc.1995-03-14400
K950304DESERET (R) T-PORT (R) MULTI FLO(TM) AND DESERET (R)PRN ADAPBecton Dickinson Vascular Access, Inc.1995-03-14480
K950302E-Z SET(R) AND MINICATH(R) INFUSION SETSBecton Dickinson Vascular Access, Inc.1995-03-13470
K942045INSYTE INTRODUCER CATHETERBecton Dickinson Vascular Access, Inc.1995-01-092560
K941429IV CATHETER AND OBTURATORBecton Dickinson Vascular Access, Inc.1995-01-042860
K943941SAFESTART VASCULAR ACCESS START KITBecton Dickinson Vascular Access, Inc.1994-10-20690
K941283INNERSENSE DISPOSABLE MICROTRANSDUCERBecton Dickinson Vascular Access, Inc.1994-04-19330
K923702INTIMA POINT GUARD INTRAVASCULAR CATHETERBecton Dickinson Vascular Access, Inc.1993-09-224250
K924737INNERSENSE(TM) DISPOSABLE MICROTRANSDUCERBecton Dickinson Vascular Access, Inc.1993-08-233350
K921845INSYTE ARTCATH ARTERIAL CATHETERIZATION UNITBecton Dickinson Vascular Access, Inc.1992-11-102070
K914528SAFEDWEL(R) CENTRAL VENOUS CATHETERBecton Dickinson Vascular Access, Inc.1992-10-133700
K914180DESERET(R) FLOW RESTRICTION VALVEBecton Dickinson Vascular Access, Inc.1992-05-082330

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda