FGY

2 FDA 510(k) clearances · Product code

FDA profile

Official device name

Cannula, Injection

Device class

Class I (low risk)

Regulation

21 CFR 878.4200

Medical specialty

General, Plastic Surgery

Adverse events (MAUDE)

1998: 5 · 1999: 1 · 2000: 2 · 2001: 2 · 2002: 2 · 2004: 2
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.

Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free