# K001373: Liquichek Immunoassay Plus Control, Model 360, 361, 362, 363

- Pathway: 510(k) (Traditional)
- Applicant: Bio-Rad
- Decided: May 25, 2000 after 24 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.
6 later devices descend from it; 5 cite it directly.
0 of 7 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
- K132091: Multichem IA and IA Plus (2013), 1 descendant of its own
- K033366: Liquichek Qualitative Urine Toxicology Control, Negative, Model 454; Positive, Model 455 (2003), 1 descendant of its own
- K162530: Multichem IA Plus (2017), 0 descendants of its own
- K132227: Liquichek Immunoassay Premium Control-Trilevel, Liquichek Immunoassay Premium Control-Level I, Liquichek Immunoassay (2013), 0 descendants of its own
- K122838: Liquickek Immunoassay Plus Control, Level 1 Model 267, Liquichek Immunoassay Plus Control, Level 2 Model 268, Liquichek (2012), 0 descendants of its own

Source page: https://510kreport.com/device/K001373
Methodology: https://510kreport.com/methodology