BYR
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Transducer, Gas Pressure, Differential
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 868.2875
- Medical specialty
- Anesthesiology
- Adverse events (MAUDE)
- 2001: 1 · 2003: 1
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 |
|---|---|---|
| BICORE VARIFLEX(R) FLOW TRANSDUCER (K896718) | Bicore Monitoring Systems | 1990-02-22 |
| MMI/GAELTEC SERIES 8T DIFF. PRESS. TRANS (K801880) | Medical Measurements, Inc. | 1980-08-14 |
| DRAGER ORM (K790334) | Draeger Medical, Inc. | 1979-03-07 |
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Every clearance here is in the API, with alerts when new ones post.