# K781939: Reagent Kit, Triglycerides

- Pathway: 510(k) (Traditional)
- Applicant: Beckman Instruments, Inc.
- Decided: Jan 10, 1979 after 51 days
- Product code: CDT (Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides)
- Device class: 1
- Regulation: 21 CFR 862.1705
- 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; 2 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
- K012221: Safe at Home Cholesterol Profile Blood Collection and Transport System (2002), 1 descendant of its own
- K063852: Accessa Cholesterol Panel (2007), 0 descendants of its own
- K011970: Biosafe Cholesterol Profile Blood Collection and Transport System (2001), 0 descendants of its own

Source page: https://510kreport.com/device/K781939
Methodology: https://510kreport.com/methodology