# Image-Intensified Fluoroscopic X-Ray System, Mobile
> **Product code: OXO** · Class II — Moderate Risk (510(k) clearance required) · Radiology · 21 CFR 892.1650
## Classification
- **FDA Product Code:** OXO
- **Device class:** Class II — Moderate Risk (510(k) clearance required)
- **Regulation:** 21 CFR 892.1650
- **Review panel:** RA
- **Medical specialty:** Radiology
- **Submission type:** 1
- **GMP exempt:** N
- **Life sustaining:** N
- **Implant:** N
- **Third-party review:** Y
## Definition

Fluoroscopy of the human body.

## Market data
- **Cleared 510(k) submissions:** 81
- **Registered establishments:** 67
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=OXO)
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