# K860204: Angiomat 6000

- Pathway: 510(k) (Traditional)
- Applicant: Mallinckrodt Group, Inc.
- Decided: May 2, 1986 after 100 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.
4 later devices descend from it; 2 cite it directly.
0 of 5 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
- K963071: Angiomat Illumena (1997), 3 descendants of its own
- K092896: Rempress and Angiography Contrast Delivery System Rempress (2010), 1 descendant of its own
- K173450: PRESS DUO elite, PRESS DUO elite AG (2018), 0 descendants of its own
- K082212: Syringe with Handi-Fil (2009), 0 descendants of its own

Source page: https://510kreport.com/device/K860204
Methodology: https://510kreport.com/methodology