# K950301: Angiocath (R) Nonvalon (R) and Angio-Set (R) IV Catheters

- Pathway: 510(k) (Traditional)
- Applicant: Becton Dickinson Vascular Access, Inc.
- Decided: Apr 18, 1995 after 83 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.
17 later devices descend from it; 2 cite it directly.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K111366: BD Nexiva Diffusics Closed IV Catheter System (2011), 13 descendants of its own
- K123734: BD Nexiva Diffusics Closed IV Catheter System (2013), 12 descendants of its own
- K161777: BD Nexiva and BD Nexiva Diffusics Closed IV Catheter Systems (2016), 11 descendants of its own
- K170336: BD Nexiva Closed IV Catheter System (Single Port) with MaxZero Needleless Connector (2017), 6 descendants of its own
- K183399: BD Nexiva Closed IV Catheter System (2019), 5 descendants of its own

Source page: https://510kreport.com/device/K950301
Methodology: https://510kreport.com/methodology