LNN
2 FDA 510(k) clearances · Product code
FDA profile
- Adverse events (MAUDE)
- 1996: 1 · 1998: 2 · 1999: 1 · 2002: 2 · 2003: 3 · 2008: 3
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
| Record | Firm | Date |
|---|---|---|
| MODEL 500-6 RADIATION THERAPY IONIZATION CHAMBER (K932342) | Victoreen, Inc. | 1993-12-13 |
| VIBROMETRY SYSTEM (K901881) | Bruel & Kjaer Instruments, Inc. | 1991-05-31 |
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Every clearance here is in the API, with alerts when new ones post.