# K240130: Medical Monitor (21HQ613D)

- Pathway: 510(k) (Special)
- Applicant: Lg Electronics.Inc
- Decided: Feb 15, 2024 after 29 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). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K221061: 21HQ613D, Lg Electronics.Inc (2022) Summary page 6.

## Indications for use
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/K240130
Methodology: https://510kreport.com/methodology