IXC
18 FDA 510(k) clearances · Product code
41 daysmedian time to decision
89 days90th percentile
18clearances measured
FDA profile
- Official device name
- Illuminator, Radiographic-Film
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 892.1890
- Medical specialty
- Radiology
- Adverse events (MAUDE)
- 1998: 1
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
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Track IXC automatically
Every clearance here is in the API, with alerts when new ones post.