# K926272: Beckman Transferrin Kit

- Pathway: 510(k) (Traditional)
- Applicant: Beckman Instruments, Inc.
- Decided: Oct 7, 1993 after 293 days
- Product code: DDG (Transferrin, Antigen, Antiserum, Control)
- Device class: 2
- Regulation: 21 CFR 866.5880
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 4 cite it directly.
0 of 10 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
- K972840: N Antiserum to Human Transferrin (1997), 4 descendants of its own
- K053075: N Antisera to Human Transferrin (2006), 3 descendants of its own
- K973928: Beckman Urine Protein Calibrator (Ucal) (1997), 1 descendant of its own
- K182095: Tina-quant Transferrin ver.2 (urine application) (2018), 0 descendants of its own
- K081299: Dimension Vista System TRF Flex Reagent Cartridge, Dimension Vista System Protein 1 Calibrator, and Dimension Vista (2008), 0 descendants of its own

Source page: https://510kreport.com/device/K926272
Methodology: https://510kreport.com/methodology