# K960392: CDM

- Pathway: 510(k) (Traditional)
- Applicant: Bio-Rad
- Decided: Jul 8, 1996 after 161 days
- Product code: LDM (Instrumentation, High Pressure Liquid Chromatography)
- Device class: 1
- Regulation: 21 CFR 862.2260
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K833113 (1983). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K833113: Reporting Integrator 3392A, Hewlett-Packard Co. (1983) Summary page 1.

## Indications for use
A software package and instrument interface that is used for quantitative analyses of high performance liquid chromatography (HPLC) test kits.

Source page: https://510kreport.com/device/K960392
Methodology: https://510kreport.com/methodology