# K921255: Philips BV26 Mobile C-Arm Stand

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems, Inc.
- Decided: May 18, 1992 after 63 days
- Product code: OXO (Image-Intensified Fluoroscopic X-Ray System, Mobile)
- Device class: 2
- Regulation: 21 CFR 892.1650
- Recalls of this device: 2 (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. The FDA summary names no predicate by number.

## Recalls of this device
- Jul 20, 2004 · Not classified · Z-1455-04: Potential for c-arm to move due to loose screws
- Jul 20, 2004 · Not classified · Z-1454-04: Potential for c-arm to move due to loose screws

Source page: https://510kreport.com/device/K921255
Methodology: https://510kreport.com/methodology