# K034054: Pro Series Couch Software, Model MT-PRO100

- Pathway: 510(k) (Traditional)
- Applicant: Med-Tec,Inc.
- Decided: Feb 20, 2004 after 52 days
- Product code: JAI (Couch, Radiation Therapy, Powered)
- Device class: 2
- Regulation: 21 CFR 892.5770
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K122201: Protura Couch Software (2012), 0 descendants of its own

## Indications for use
The intended use of this device is to: Interface between treatment planning system and the MED-TEC Pro Series Couch; or: Software for MED-TEC Pro Series Couch (6 Degree Axis Couch).

Source page: https://510kreport.com/device/K034054
Methodology: https://510kreport.com/methodology