# K904219: Synchron CX 7 Clinical Analyzer

- Pathway: 510(k) (Traditional)
- Applicant: Beckman
- Decided: Oct 22, 1990 after 40 days
- Product code: JJE (Analyzer, Chemistry (Photometric, Discrete), For Clinical Use)
- Device class: 1
- Regulation: 21 CFR 862.2160
- 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; 3 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
- K112377: BS-400 Chemistry Analyzer, CLC 720 Chemistry Analyzer (2012), 1 descendant of its own
- K140690: BS-480 Chemistry Analyzer, BS-490 Chemistry Analyzer, CLC720I Chemistry Analyzer (2014), 0 descendants of its own
- K103531: Prestige 24I; Biolis 24I; MGC 240 (2011), 0 descendants of its own
- K971505: Synchron Systems Cholesterol (Chol) Reagent (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K904219
Methodology: https://510kreport.com/methodology