# K972966: Axt 150M Manual Collimator (Axt 150M)

- Pathway: 510(k) (Traditional)
- Applicant: Applied X-Ray Technologies, Inc.
- Decided: Aug 21, 1997 after 10 days
- Product code: IZX (Collimator, Manual, Radiographic)
- Device class: 2
- Regulation: 21 CFR 892.1610
- 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
- K073124: Collimare Collimator Family (2007), 0 descendants of its own

## Indications for use
The AXT 150M and/or variations is intended to be used by or under the authority of a licensed MD or RT. The AXT 150M and/or its variations is used to control the x-ray beam for use on a diagnostic imaging equipment. The intended market will consist of Original Equipment Manufactures (OEM), Re-manufactures/Rebuilders and Independent X-Ray Dealers. The unit is designed to be adapted to various x-ray systems.

Source page: https://510kreport.com/device/K972966
Methodology: https://510kreport.com/methodology