510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K172738Substantially Equivalent

RadiForce RX560, RX560-AR

Eizo Corporation, Hakusan, JP / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K172738 is the FDA 510(k) clearance record for RadiForce RX560, RX560-AR, a class II device, cleared for Eizo Corporation on under FDA product code PGY (Display, Diagnostic Radiology). FDA's definition for product code PGY reads: "The device is intended for use in displaying radiological images for review, analysis, and diagnosis by trained medical practitioners". FDA records list 23 510(k) clearances for Eizo Corporation, from to . As of , FDA records show no recalls naming K172738.

Clearance record

Decision date
Received
(57 days to decision)
Product code
PGY Display, Diagnostic Radiology
Regulation
21 CFR 892.2050
Device class
Class II
Review panel
Radiology
Applicant
Eizo Corporation 153 Shimokashiwano, Hakusan, JP
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PGY

Trailing 12 months
3 clearances under product code PGY in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code PGY, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20261
October 20260