A1417MCW/A1717MCW/F1417MCW

FDA 510(k) K223930 · H&abyz Co., Ltd.

Substantially Equivalent

510(k) numberK223930

Submission

Device name
A1417MCW/A1717MCW/F1417MCW
Applicant
H&abyz Co., Ltd.
Yongin-Si, KR
Received
December 30, 2022
Decision date
March 6, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MQB – Solid State X-Ray Imager (Flat Panel/Digital Imager)
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1680
Specialty
Radiology

Other 510(k)s with product code MQB

510(k)DeviceApplicantDecision
K2538000909FCE, 0909FCE-HSMQB · Traditional Rayence Co., Ltd.07/31/2026SE
K260820Vivix-S 4386W (FXRD-4386WA)MQB · Special Vieworks Co., Ltd.06/18/2026SE
K252996Universal 1417PIMQB · Abbreviated Konica Minolta Healthcare Americas, Inc.06/12/2026SE
K252911Lux HD 2530 detector (Lux HD 2530)MQB · Special Iray Imaging Technology (Haining) Limited10/09/2025SE
K250211Yushan X-Ray Flat Panel DetectorMQB · Traditional Innocare Optoelectronics Corp.07/22/2025SE
K250665SKR 3000MQB · Traditional Konica Minolta, Inc.06/17/2025SE
K243734Wireless/ Wired X-Ray Flat Panel DetectorsMQB · Special Allengers Medical Systems Limited04/18/2025SE
K242770Expd 114; Expd 114G; Expd 114P; Expd 114PGMQB · Special DRTECH Corporation03/20/2025SE
K243443Expd 4343N1; Expd 4343N; Expd 4343U1; Expd 4343NU; Expd 4343NP; Expd 3643N1; Expd 3643N…MQB · Special DRTECH Corporation03/19/2025SE
K243556Lux HD 35 Detector (Lux HD 35); Lux HD 43 Detector (Lux HD 43)MQB · Traditional Iray Imaging Technology (Haining) Limited03/18/2025SE

More from Iray Imaging Technology (Haining) Limited

510(k)DeviceDecision
K251223HnX-P1, HnX-PBIZL · Traditional 08/04/2025SE
K213497ADD (Model Name: HAD1417MCW), ADD (Model Name: HAD1717MCW)MQB · Special 11/15/2021SE
K203188AddMQB · Traditional 03/12/2021SE
K200018HAD1717MCMQB · Traditional 01/31/2020SE

Questions and answers

When was A1417MCW/A1717MCW/F1417MCW cleared by the FDA?

A1417MCW/A1717MCW/F1417MCW (K223930) received a 510(k) decision of Substantially Equivalent on March 6, 2023, 66 days after the submission was received.

What is the product code of K223930?

The FDA product code is MQB – Solid State X-Ray Imager (Flat Panel/Digital Imager), a Class II (moderate risk) device regulated under 21 CFR 892.1680.