IZT

1 FDA 510(k) clearances · Product code

FDA profile

Official device name

Cone, Radiographic

Device class

Class II (moderate risk)

Regulation

21 CFR 892.1610

Medical specialty

Radiology

Adverse events (MAUDE)

2001: 1
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.

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