# K924453: Multi-Channel Discrete Analyzer (Mda-180)

- Pathway: 510(k) (Traditional)
- Applicant: Organon Teknika Corp.
- Decided: Dec 18, 1992 after 107 days
- Product code: JPA (System, Multipurpose For In Vitro Coagulation Studies)
- Device class: 2
- Regulation: 21 CFR 864.5425
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 3 cite it directly.
0 of 4 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
- K962857: Coag-a-Mate MTX (1997), 2 descendants of its own
- K051030: Coag-a-Mate MTX Iii (2005), 0 descendants of its own
- K033137: Potens + (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K924453
Methodology: https://510kreport.com/methodology