# K000482: Modification to Autoject Mini

- Pathway: 510(k) (Traditional)
- Applicant: Owen Mumford, Ltd.
- Decided: Mar 6, 2000 after 21 days
- Product code: KZH (Introducer, Syringe Needle)
- Device class: 2
- Regulation: 21 CFR 880.6920
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 2 cite it directly.
0 of 8 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
- K050434: SHL Disposable Autoinjector (2005), 4 descendants of its own
- K060141: DAI-R (2006), 3 descendants of its own
- K070100: Haselmeier Pen (2007), 2 descendants of its own
- K073476: Compact Auto-Safety Injector (Casi) (2008), 1 descendant of its own
- K083457: Tactipen (2009), 0 descendants of its own

Source page: https://510kreport.com/device/K000482
Methodology: https://510kreport.com/methodology