# K953735: Autoject Mini

- Pathway: 510(k) (Traditional)
- Applicant: Owen Mumford USA, Inc.
- Decided: Nov 8, 1995 after 90 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K042557: Innoject Auto-Injector (2004), 1 descendant of its own
- K060389: Confidose IM Auto-Injector (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K953735
Methodology: https://510kreport.com/methodology