ETL
4 FDA 510(k) clearances · Product code
FDA profile
- Adverse events (MAUDE)
- 1992: 1 · 1993: 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 |
|---|---|---|
| ATMOS ENT PATIENT CHAIR #5 (K791938) | Jedmed Instrument Co. | 1979-11-13 |
| ATMOS ENT PATIENT CHAIR #1 (K791937) | Jedmed Instrument Co. | 1979-11-13 |
| ANEMOMETER, NASAL, EXETER (K781218) | Medika Corp. | 1978-07-27 |
| NASSAL PRESSURE/FLOW RECORDER (K772193) | Adco Labs. | 1977-12-02 |
Track ETL automatically
Every clearance here is in the API, with alerts when new ones post.