KBZ

1 FDA 510(k) clearances · Product code

FDA profile

Official device name

Snare, Tonsil

Device class

Class I (low risk)

Regulation

21 CFR 874.4420

Medical specialty

Ear, Nose, Throat

Adverse events (MAUDE)

1996: 2 · 1997: 2 · 1999: 2 · 2000: 3 · 2003: 3 · 2008: 3
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.

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