# K123499: Aeropilot

- Pathway: 510(k) (Traditional)
- Applicant: Konica Minolta Medical & Graphic, Inc.
- Decided: Dec 20, 2012 after 37 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: 7 generations back to K981556 (1998). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102349: Aerodr System, Konica Minolta Medical & Graphic, Inc. (2010) Summary page 1.
- K120477: Aerosync for Aerodr System, Konica Minolta Medical & Graphic, Inc. (2012) Summary page 2.
- K113248: Aerodr System with P-21, Konica Minolta Medical & Graphic, Inc. (2012) Summary page 1.

## Indications for use
AeroPilot is a software device that is used in conjunction with REGIUS Unitea to control Konica Minolta Digital Radiography systems. This device is indicated for use in generating radiographic images of human anatomy. It is intended to replace radiographic film/screen systems in general-purpose diagnostic procedures. This device is not indicated for use in mammography, fluoroscopy, tomography and angiography applications.

Source page: https://510kreport.com/device/K123499
Methodology: https://510kreport.com/methodology