# K002471: Jetcan Huber Neeedle Set

- Pathway: 510(k) (Traditional)
- Applicant: Pfm Produkte Fur Die Medizin AG
- Decided: Oct 19, 2000 after 69 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.
10 later devices descend from it; 1 cites it directly.
0 of 11 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
- K040533: EZ Huber Safety Infusion Set (2004), 9 descendants of its own
- K071846: Modification to EZ Huber Safety Infusion Set (2007), 8 descendants of its own
- K080544: Unassigned (2008), 6 descendants of its own
- K132880: Medcomp Power Injectable Safety Huber Needle (2014), 2 descendants of its own
- K111101: Norport CT-PC, Lucent Non-Coring Needel Infusion Set (2011), 2 descendants of its own

Source page: https://510kreport.com/device/K002471
Methodology: https://510kreport.com/methodology