FDA product code GZN
Rheoencephalograph
Neurology·Class 3·21 CFR 882.1825
US regulatory classifications
- US Product Code (FDA)
- GZNView Product Code Classification →
- US Risk Class (FDA)
- Class 3
- US Regulation (CFR)
- 21 CFR 882.1825View CFR Regulation →
- Medical specialty
- Neurology
Device characteristics
- GMP exempt
- No
- Implantable
- No
- Life-sustaining
- No
- Third party review
- Not Eligible
Definition
Call for PMAs to be filed by 12/26/96 per 61 FR 50708 on 9/27/96
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About this record
Rheoencephalograph is a medical device type in the Neurology 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.