# K212295: 21HQ513D

- Pathway: 510(k) (Traditional)
- Applicant: Lg Electronics.Inc
- Decided: Dec 3, 2021 after 134 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: 6 generations back to K033466 (2004). 6 ancestors in all.
4 later devices descend from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K191864: 21HK512D, Lg Electronics.Inc (2019) Summary page 6.

## Most influential descendants
- K223789: 21HQ513D (2023), 3 descendants of its own
- K232127: 21HQ513D, 32HL512D, 31HN713D, 32HQ713D (2023), 1 descendant of its own
- K261213: Medical Monitor (40HT513D) (2026), 0 descendants of its own
- K232985: 24HR513C (2023), 0 descendants of its own

## Indications for use
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.

Source page: https://510kreport.com/device/K212295
Methodology: https://510kreport.com/methodology