# K030255: Silicone Dual Lumen Radpicc Catheters

- Pathway: 510(k) (Special)
- Applicant: C.R. Bard, Inc.
- Decided: Feb 7, 2003 after 14 days
- Product code: LJS (Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days)
- Device class: 2
- Regulation: 21 CFR 880.5970
- 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 K954104 (1995). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K954104: Per-Q-Cath & Per-Q-Cath Dual Mumen Catheters, Trays & Accessory Devices, C.R. Bard, Inc. (1995) Summary page 3.

## Indications for use
The RadPICCs are indicated for short or long term peripheral access to the central venous system for intravenous therapy and blood sampling. For blood therapy, utilize the larger lumen.

Source page: https://510kreport.com/device/K030255
Methodology: https://510kreport.com/methodology