# K930272: Hemagen Chagas' Kit (Eia Method)

- Pathway: 510(k) (Traditional)
- Applicant: Hemagen Diagnostics, Inc.
- Decided: May 19, 1995 after 850 days
- Product code: MIU (Enzyme Linked Immunosorbent Assay, T. Cruzi)
- Device class: 1
- Regulation: 21 CFR 866.3870
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K072732: Ortho T. Cruzi Elisa Test System (2009), 0 descendants of its own

Source page: https://510kreport.com/device/K930272
Methodology: https://510kreport.com/methodology