# K102474: Flaatz 750E

- Pathway: 510(k) (Traditional)
- Applicant: Drtech Corp.
- Decided: Mar 4, 2011 after 186 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: 2 generations back to K063710 (2007). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K080064: Flaatz 750, Drtech Corp. (2008) Summary page 1.

## Indications for use
The FLAATZ 750E is indicated for use in generating radiographic images of human anatomy. It is intended to replace radiographic film/screen systems in all general-purpose diagnostic procedures. (excluding fluoroscopic, angiographic, and mammographic applications).

Source page: https://510kreport.com/device/K102474
Methodology: https://510kreport.com/methodology