# K073476: Compact Auto-Safety Injector (Casi)

- Pathway: 510(k) (Traditional)
- Applicant: Medical House (Asi) Limited
- Decided: Mar 7, 2008 after 88 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
Longest line of descent: 1 generation back to K000482 (2000). 1 ancestor in all.
1 later device descends 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)
- K000482: Modification to Autoject Mini, Owen Mumford, Ltd. (2000) Summary page 1.

## Most influential descendants
- K082587: Auto-Safety Injector-2 (Asi-2) (2008), 0 descendants of its own

## Indications for use
The Compact Auto Safety Injector (CASI) is indicated for assisting the self-administered subcutaneous injection of fixed doses of FDA approved drug products with viscous liquid formulations, which are presented in standard 1 ml long BD Hypak® pre-filled syringes with staked needles. The CASI is primarily intended for home use by patients to aid and support their treatment regime or may be used by Health Care Professionals or caregivers.

Source page: https://510kreport.com/device/K073476
Methodology: https://510kreport.com/methodology