# K952861: Angiocath & Insyte Autoguard Catheters

- Pathway: 510(k) (Traditional)
- Applicant: Becton Dickinson Vascular Access, Inc.
- Decided: Jul 31, 1995 after 39 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.
5 later devices descend from it; 2 cite it directly.
0 of 6 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
- K223018: OSPREY PERIPHERAL IV Catheter System (2023), 2 descendants of its own
- K231626: OSPREY Closed IV Catheter System (OspreyV2) (2023), 1 descendant of its own
- K201075: BD Insyte Autoguard Shielded IV Catheter, BD Insyte Autoguard BC Shielded IV Catheter, BD Insyte Autoguard BC Pro Shielded IV Catheter (2020), 1 descendant of its own
- K251654: BD Insyte™ Autoguard™ Shielded IV Catheter, BD Insyte™ Autoguard™ BC Shielded IV Catheter and BD Insyte™ Autoguard™ BC Pro Shielded IV Catheter (2025), 0 descendants of its own
- K250292: OSPREY Midline Closed IV Catheter System  (OspreyEDC-F20) (2025), 0 descendants of its own

Source page: https://510kreport.com/device/K952861
Methodology: https://510kreport.com/methodology