# K223930: A1417MCW/A1717MCW/F1417MCW

- Pathway: 510(k) (Traditional)
- Applicant: H&abyz Co., Ltd.
- Decided: Mar 6, 2023 after 66 days
- Product code: MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager))
- Device class: 2
- Regulation: 21 CFR 892.1680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 19 generations back to K981556 (1998). 85 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 87 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K213497: ADD (Model Name: HAD1417MCW), ADD (Model Name: HAD1717MCW), H&abyz Co., Ltd. (2021) Summary page 5.

## Most influential descendants
- K241346: IODR1717 / IODR1417 / IODR1417-GF  (Digital Flat Panel X-ray Detector) (2024), 0 descendants of its own

## Indications for use
A1417MCW / A1717MCW / F1417MCW (Digital Flat Panel X-Ray Detector) are indicated for digital imaging solution designed for providing general radiographic diagnosis of human anatomy targeting both adult and children. It is intended to replace film based radiographic diagnostic systems. Not to be used for mammography.

Source page: https://510kreport.com/device/K223930
Methodology: https://510kreport.com/methodology