← FDA Medical Device Classifications
System, X-Ray, Angiographic
IZI · Class II — Moderate Risk (510(k) clearance required) · Radiology · 21 CFR 892.1600
Classification
- FDA Product Code
IZI- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 892.1600
- Review panel
- RA
- Medical specialty
- Radiology
- Submission type
- 1
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- N
Market data
- Cleared 510(k) submissions
- 197
- Registered establishments
- 123
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown