# K100775: BD Intima II Closed IV Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Becton Dickinson Infusion Therapy Systems, Inc.
- Decided: Jun 3, 2010 after 77 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
Longest line of descent: 1 generation back to K833657 (1983). 2 ancestors in all.
3 later devices descend from it; 1 cites 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)
- K833657: Angio-Set Intravenous Cath. Set, Deseret Medical, Inc. (1983) Summary page 1.
- K843033: Deseret Intravascular Catheter, Parke-Davis Co. (1984) Summary page 1.

## Most influential descendants
- 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

## Indications for use
The BID Intima 11IV Catheter is inserted into a patient's vascular system for short-term use to monitor blood pressure or administer fluids intravascularly.

Source page: https://510kreport.com/device/K100775
Methodology: https://510kreport.com/methodology