# K843033: Deseret Intravascular Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Parke-Davis Co.
- Decided: Dec 3, 1984 after 124 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.
4 later devices descend from it; 1 cites it directly.
0 of 5 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
- K100775: BD Intima II Closed IV Catheter (2010), 3 descendants of its own
- K143610: BD Intima II Closed IV Catheter (2015), 2 descendants of its own
- K172204: BD Intima II PLUS Closed IV Catheter System (2017), 1 descendant of its own
- K200891: BD Intima II Closed IV Catheter System, BD Intima II PLUS Closed IV Catheter System (2021), 0 descendants of its own

Source page: https://510kreport.com/device/K843033
Methodology: https://510kreport.com/methodology