# K071691: Dual Shot Alpha

- Pathway: 510(k) (Special)
- Applicant: Nemoto Kyorindo Co., Ltd.
- Decided: Dec 19, 2007 after 182 days
- Product code: DXT (Injector And Syringe, Angiographic)
- Device class: 2
- Regulation: 21 CFR 870.1650
- 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
- K133189: Dual Shot Alpha 7 (2014), 1 descendant of its own
- K173450: PRESS DUO elite, PRESS DUO elite AG (2018), 0 descendants of its own

Source page: https://510kreport.com/device/K071691
Methodology: https://510kreport.com/methodology