KGA
1 FDA 510(k) clearances · Product code
FDA profile
- Adverse events (MAUDE)
- 2000: 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 |
|---|---|---|
| SEIZURE EMERGENCY EQUIPMENT KIT; SEIZURE KIT (K973176) | Lotus Technologies | 1997-11-21 |
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Every clearance here is in the API, with alerts when new ones post.