# K193243: Alta Multipurpose Device

- Pathway: 510(k) (Traditional)
- Applicant: Qfix
- Decided: Feb 28, 2020 after 95 days
- Product code: IYE (Accelerator, Linear, Medical)
- Device class: 2
- Regulation: 21 CFR 892.5050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K905007 (1991). 18 ancestors in all.
No later device cites it as a predicate yet.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K142420: Patient Positioning Devices, Macromedics BV (2015) Summary page 6.

## Indications for use
The Alta™ Multipurpose Device is intended to immobilize, support, position, and transfer patients undergoing radiotherapy procedures using electrons, photons, protons, including SBRT and SRS; imaging procedures such as X-ray, computed tomography, and magnetic resonance imaging; and other procedures involving transfer of a patient. The Alta™ Multipurpose Device is designed to interface with the Symphony® Patient Transport System and other positioning devices, such as couch tops, thermoplastic masks, setup-specific treatment devices and adapters, and positioning supports and pads.

Source page: https://510kreport.com/device/K193243
Methodology: https://510kreport.com/methodology