# K850198: Floor to Wall or Floor to Ceiling Tubestand;Radiog

- Pathway: 510(k) (Traditional)
- Applicant: Summit Industries, Inc.
- Decided: May 14, 1985 after 116 days
- Product code: IYB (Tube Mount, X-Ray, Diagnostic)
- Device class: 1
- Regulation: 21 CFR 892.1770
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Recalls of this device
- Oct 28, 2014 · Class II · Z-0468-2015: The welds on J700 tube stands may be insufficient resulting in tube stand breakage, damage to the X-Ray machine, and/or patient or healthcare provider injury.

Source page: https://510kreport.com/device/K850198
Methodology: https://510kreport.com/methodology