# K923702: Intima Point Guard Intravascular Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Becton Dickinson Vascular Access, Inc.
- Decided: Sep 22, 1993 after 425 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; 3 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
- K082997: Terumo Hybria Closed System Safety I.V. Catheter (2009), 4 descendants of its own
- K100282: Terumo Surshield- Pur Safety I.V. Catheter (2010), 3 descendants of its own
- K122544: Terumo Surflash Safety I.V. Catheter (2012), 1 descendant of its own
- K141138: Surflash Safety I.V. Catheter (2014), 0 descendants of its own
- K123267: Surfflash (R) Plus Safety I.V. Catheter (2012), 0 descendants of its own

Source page: https://510kreport.com/device/K923702
Methodology: https://510kreport.com/methodology