# K002799: Paragon Cze 2000 Capillary Electrophoresis System and Buffer-100

- Pathway: 510(k) (Special)
- Applicant: Beckman Coulter, Inc.
- Decided: Oct 5, 2000 after 27 days
- Product code: CFF (Immunoelectrophoretic, Immunoglobulins, (G, A, M))
- Device class: 2
- Regulation: 21 CFR 866.5510
- 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; 1 cites 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
- K130500: Capillarys Immunotyping, Capillarys 2 Instrument, IT/IF Control, Capillarys 2 Flex Piercing Instrument (2013), 2 descendants of its own
- K161928: Capi 3 Immunotyping, Capillarys 3 Tera, IT/IF Control (2016), 1 descendant of its own
- K192095: CAPI 3 Immunotyping, Capillarys 3 Tera (2019), 0 descendants of its own

Source page: https://510kreport.com/device/K002799
Methodology: https://510kreport.com/methodology