# K042862: BD Onecath

- Pathway: 510(k) (Traditional)
- Applicant: Becton Dickinson Infusion Therapy Systems, Inc.
- Decided: Dec 3, 2004 after 49 days
- Product code: FOZ (Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days)
- Device class: 2
- Regulation: 21 CFR 880.5200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
26 later devices descend from it; 1 cites it directly.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) BD L-Cath Midline Catheter: named in the summary without a submission number

## Most influential descendants
- K101422: The Power Wand Safety Introducer with an Extended Dwell Catheter (2011), 25 descendants of its own
- K121073: Powerglide Midline Catheter (2012), 19 descendants of its own
- K133856: Powerglide Midline Catheter (2014), 12 descendants of its own
- K153280: PowerGlide Pro Midline Catheter (2016), 5 descendants of its own
- K150407: BioFlo Midline Catheter (2015), 5 descendants of its own

## Indications for use
The BD OneCathTM midline catheter is inserted into a patient's vascular system for short-term use (less than 30 days) to sample blood, monitor blood pressure, or administer fluids. This intravascular catheter may be used for any patient population with consideration given to adequacy of vascular anatomy and appropriateness of procedure.

Source page: https://510kreport.com/device/K042862
Methodology: https://510kreport.com/methodology