# K953077: Paragon Cze 2000 Clinical Capillary Electrophoresis System

- Pathway: 510(k) (Traditional)
- Applicant: Beckman Instruments, Inc.
- Decided: Jan 5, 1996 after 189 days
- Product code: CDF (Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin)
- Device class: 1
- Regulation: 21 CFR 862.1795
- 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
- K963018: Bio-Rad Serum Proteins by Capillary Electrophoresis (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K953077
Methodology: https://510kreport.com/methodology