BRY
5 FDA 510(k) clearances · Product code
26 daysmedian time to decision
82 days90th percentile
5clearances measured
FDA profile
- Official device name
- Cabinet, Table And Tray, Anesthesia
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 868.6100
- Medical specialty
- Anesthesiology
- Adverse events (MAUDE)
- 2021: 57 · 2022: 199 · 2023: 314 · 2024: 1,600 · 2025: 61,848 · 2026: 33,479
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 |
|---|---|---|
| MOVIT DEVICE (K921710) | John J. Navar, M.D. | 1992-06-29 |
| MEDIKEEPER (K912346) | Medikeeper, Inc. | 1991-07-30 |
| ANESTHESIA WORKSTATION (K901474) | Siemens Life Support Systems | 1990-04-10 |
| ANESTHASSIST (K871564) | Anestech, Inc. | 1987-05-18 |
| ANESTHECACHE (K821307) | Med-Life, Inc. | 1982-05-14 |
Track BRY automatically
Every clearance here is in the API, with alerts when new ones post.