# K833113: Reporting Integrator 3392A

- Pathway: 510(k) (Traditional)
- Applicant: Hewlett-Packard Co.
- Decided: Nov 21, 1983 after 69 days
- Product code: LDM (Instrumentation, High Pressure Liquid Chromatography)
- Device class: 1
- Regulation: 21 CFR 862.2260
- Recalls of this device: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K960392: CDM (1996), 0 descendants of its own

## Recalls of this device
- Nov 17, 2003 · Not classified · Z-0324-04: Drug product cross reacts with the Tricyclic Antidepressants (TCA) assay.
- Dec 11, 2002 · Not classified · Z-0690-03: Unexpected false positive TCA results

Source page: https://510kreport.com/device/K833113
Methodology: https://510kreport.com/methodology