# K973177: Mago Automated Eia Processor

- Pathway: 510(k) (Traditional)
- Applicant: Diamedix Corp.
- Decided: Oct 9, 1997 after 45 days
- Product code: JJF (Analyzer, Chemistry, Micro, For Clinical Use)
- Device class: 1
- Regulation: 21 CFR 862.2170
- 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. The FDA summary names its predicate without a number.
- (no number) Rosys Plato 3300: named in the summary without a submission number

## Most influential descendants
- K052794: Eti-Max 3000 (2006), 0 descendants of its own

## Indications for use
The Diamedix MAGO is indicated for use as a general purpose automated EIA processor for use in clinical laboratories.

Source page: https://510kreport.com/device/K973177
Methodology: https://510kreport.com/methodology