# K011033: Dimension Lithium (LI) Flex Reagent Cartridge, Model DF 132

- Pathway: 510(k) (Traditional)
- Applicant: Dade Behring, Inc.
- Decided: Jun 7, 2001 after 63 days
- Product code: JIH (Flame Photometry, Lithium)
- Device class: 2
- Regulation: 21 CFR 862.3560
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K112142: Dimension Vista Lithium Flex Reagent Cartridge (2011), 0 descendants of its own
- K061792: Dimension Vista Ethyl Alcohol (Alc), Alkaline Phosphatase (Alp), Calcium (CA0 Flex, Lactic Acid (LA) Flex Reagent Cartri (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K011033
Methodology: https://510kreport.com/methodology