# K070968: Choy Compression Frame

- Pathway: 510(k) (Traditional)
- Applicant: Choy Medical Technologies, Inc.
- Decided: Nov 15, 2007 after 224 days
- Product code: LNH (System, Nuclear Magnetic Resonance Imaging)
- Device class: 2
- Regulation: 21 CFR 892.1000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K992120 (1999). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K992120: Dynawell or Dynawell, Ekeroth Quality AB (1999) Summary page 2.

## Indications for use
The Choy Compression Frame is indicated as an accessory for axial compression of the lumbar spine in CT and MR diagnostic imaging.

Source page: https://510kreport.com/device/K070968
Methodology: https://510kreport.com/methodology