# K230845: 32HL512D, 31HN713D, 32HQ713D

- Pathway: 510(k) (Special)
- Applicant: Lg Electronics.Inc
- Decided: Apr 27, 2023 after 30 days
- Product code: PGY (Display, Diagnostic Radiology)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K103792 (2011). 10 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K192925: 32HL512D, Lg Electronics.Inc (2020) Summary page 5.
- K201777: 31HN713D, Lg Electronics.Inc (2020) Summary page 5.
- K223423: 32HQ713D, Lg Electronics.Inc (2023) Summary page 5.

## Most influential descendants
- K232127: 21HQ513D, 32HL512D, 31HN713D, 32HQ713D (2023), 1 descendant of its own
- K261213: Medical Monitor (40HT513D) (2026), 0 descendants of its own

## Indications for use
32HL512D This Medical Monitor is indicated for use in displaying radiological images for review, analysis, and diagnosis by trained medical practitioners. The display is not intended for mammography. 31HN713D, 32HQ713D This Medical Monitor is indicated for use in displaying radiological images (including full-field digital mammography and digital breast tomosynthesis) for review, analysis, and diagnosis by trained medical practitioners.

Source page: https://510kreport.com/device/K230845
Methodology: https://510kreport.com/methodology