# K932076: Liquichek Spinal Fluid Control Levels I and II

- Pathway: 510(k) (Traditional)
- Applicant: Bio-Rad
- Decided: Jun 29, 1993 after 61 days
- Product code: JJY (Multi-Analyte Controls, All Kinds (Assayed))
- Device class: 1
- Regulation: 21 CFR 862.1660
- 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; 1 cites 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K990888: Modification to Liquichek Spinal Fluid Control, Item Nos. 751, 752 (1999), 1 descendant of its own
- K123775: Liquichek Spinal Fluid Control Level 1, Liquichek Spinal Fluid Control Level 2, Liquichek Spinal Fluid Control Minipak (2013), 0 descendants of its own

Source page: https://510kreport.com/device/K932076
Methodology: https://510kreport.com/methodology