MHZ
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Stimulator, Vestibular Acceleration, Therapeutic
- Device class
- Class III (high risk)
- Medical specialty
- Unknown
- Adverse events (MAUDE)
- 1992: 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 |
|---|---|---|
| TRANSDUCER FOR KONTROL 5MHZ SIGMA 20 (K843355) | Kontron Instruments, Inc. | 1984-12-03 |
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Every clearance here is in the API, with alerts when new ones post.