FDA product code PGY
Display, Diagnostic Radiology
Radiology·Class 2·21 CFR 892.2050
US regulatory classifications
- US Product Code (FDA)
- PGYView Product Code Classification →
- US Risk Class (FDA)
- Class 2
- US Regulation (CFR)
- 21 CFR 892.2050View CFR Regulation →
- Medical specialty
- Radiology
Device characteristics
- GMP exempt
- No
- Implantable
- No
- Life-sustaining
- No
- Third party review
- Eligible
Definition
The device is intended for use in displaying radiological images for review, analysis, and diagnosis by trained medical practitioners.
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About this record
Display, Diagnostic Radiology is a medical device type in the Radiology specialty. This page includes real-world medical device registration data worldwide for this device type, with registrations from US FDA, Brazil ANVISA, and other global markets.
View regulatory classifications, recent 510(k) clearances, active device registrations, and similar products registered globally under this device category. Pure Global AI's free directory provides comprehensive worldwide registration intelligence across 7,000+ medical device types and 21 specialties.