← FDA Medical Device Classifications
Fluoroscopic X-Ray Image Intensifier
QHX · Class I — Low Risk (general controls) · Radiology · 21 CFR 892.1960
Classification
- FDA Product Code
QHX- Device class
- Class I — Low Risk (general controls)
- Regulation
- 21 CFR 892.1960
- Review panel
- RA
- Medical specialty
- Radiology
- Submission type
- 4
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- N
Definition
To instantaneously convert an x-ray pattern from a fluoroscopic x-ray system into a corresponding light image of higher energy density.
Market data
- Cleared 510(k) submissions
- 0
- Registered establishments
- 0
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown