# K021471: Marquette Huber Trap Safety Infusion Set

- Pathway: 510(k) (Traditional)
- Applicant: Marquette Medical, Inc.
- Decided: Sep 8, 2003 after 488 days
- Product code: FPA (Set, Administration, Intravascular)
- Device class: 2
- Regulation: 21 CFR 880.5440
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Marquette Medical Safety Huber Infusion Set is a safety IV administration set used to access surgically implanted vascular ports. The Medical Safety Huber Needle is used to administer fluids or drugs and blood sampling. The Marquette Medical Safety Huber Infksion Set facilitates safe removal of the needle by encapsulating the needle within a telescoping plastic cone to help prevent needle-stick injuries when using the device for vascular port access.

Source page: https://510kreport.com/device/K021471
Methodology: https://510kreport.com/methodology