510(k) Report

510(k) · Cleared

Cleared

RadiForce RX270

K223768510(k) AbbreviatedCleared Apr 20, 2023126-day reviewClass II21 CFR 892.2050

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Eizo Corporation · PGY Display, Diagnostic Radiology

Cleared on Apr 20, 2023 as substantially equivalent to K160247 (Eizo Corporation, 2016) and 1 other predicate after a 126-day review. Its family tree reaches back 6 generations to 2004.

Decided
Apr 20, 2023
Review
126 days
Class
Class II
Product code
PGY
Recalls
None
Predicates
2

Its longest line of descent runs back 6 generations to K033466 (2004). 10 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 6 generations backK033466 Color LCD Display, Model Radiforce R22Eizo Nanao Corporation · 2004
  2. 5 generations backK052344 Color LCD Monitor, Model Radioforce R31 & R31-CEizo Nanao Corporation · 2005
  3. 4 generations backK090045 Color LCD Monitor, Radiforce RX320Eizo Nanao Corporation · 2009
  4. 3 generations backK113562 3MP Color LCD Monitor, Radiforce RX340Eizo Nanao Corporation · 2012
  5. 2 generations backK153354 3MP Color LCD Monitor, RadiForce RX350Eizo Corporation · 2016
  6. 1 generation backK182591 RadiForce RX360, RX360-AREizo Corporation · 2018 · Recalled
  7. This deviceK223768 RadiForce RX270Eizo Corporation · 2023
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K033466Color LCD Display, Model Radiforce R22Eizo Nanao Corporation2004—
−5K052344Color LCD Monitor, Model Radioforce R31 & R31-CEizo Nanao Corporation2005—
−4K090045Color LCD Monitor, Radiforce RX320Eizo Nanao Corporation2009—
−3K1135623MP Color LCD Monitor, Radiforce RX340Eizo Nanao Corporation2012—
−2K1533543MP Color LCD Monitor, RadiForce RX350Eizo Corporation2016—
−1K182591RadiForce RX360, RX360-AREizo Corporation20181
0 (this device)K223768RadiForce RX270Eizo Corporation2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
201010
201210
201510
201610
FIG. 1 — Lineage of K223768, 2004–2023Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in PGY? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new PGY device

  1. #1 K261213 Medical Monitor (40HT513D)score 13.9 · 9 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (2)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K1602472MP Color LCD Monitor, RadiForce RX250 and RX250-AR
Summary page 4
…(21 CFR 892.2050) • Regulatory Class: II • Product Code: PGY 3. Predicate Device • Name of Device: RadiForce RX250, RX250-AR (K160247) • Common or Usual Name: 2MP Color LCD Monitor • Classification Name: Medical image management and processing system…
Eizo Corporation2016—
*K182591RadiForce RX360, RX360-AR
Summary page 4
…em (21 CFR 892.2050) • Regulatory Class: II • Product Code: PGY • Name of Device: RadiForce RX360, RX360-AR (K182591) • Common or Usual Name: 54.1 cm (21.3 inch) class Color LCD Monitor • Classification Name: Picture archiving a…
Eizo Corporation20181
†K190153RadiForce MX216Eizo Corporation2019—
†K1533543MP Color LCD Monitor, RadiForce RX350Eizo Corporation2016—
†K1633356MP Color LCD Monitor, RadiForce RX660, RX660-AREizo Corporation2016—

Also cleared against K160247: 2 other devices →

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 19 years and passes through 2 companies; a new generation was cleared every 3.5 years on median.
  • 1 of the 10 ancestors has a recall of any class.
  • 2 other devices also cite its predicate K160247.

How does its category compare?

All PGY devices

PGY Display, Diagnostic Radiology: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · PGY

3in 2025

2014: 142015: 162016: 182017: 112018: 52019: 112020: 122021: 72022: 102023: 172024: 102025: 32026 (partial year): 4
2007high 18 (2016) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PGY

59in 2025

2014: 24 days median2015: 31 days median2016: 27 days median2017: 30 days median2018: 28 days median2019: 58 days median2020: 61 days median2021: 77 days median2022: 60 days median2023: 60 days median2024: 53 days median2025: 59 days median2026 (partial year): 48 days median
2007high 77 (2021) · low 24 (2014)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · PGY

No recall names PGY since 2007.

Adverse event reports per year · PGY

1in 2017

2017: 1
2007high 1 (2017) · low 0 (2007)2025

MAUDE reports naming product code PGY, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
2014142400
2015163100
2016182700
2017113001
201852800
2019115800
2020126100
202177700
2022106000
2023176000
2024105300
202535900
20264480—

What is it indicated for?

This Product is indicated for use in displaying radiological images for review, analysis, and diagnosis by trained medical practitioners. The display is not intended for mammography.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K223768: RadiForce RX270.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K223768

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026