Electromed, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
Advertisement
Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K222496 | Electromed SmartVest Airway Clearance System | BYI | 2022-11-18 | View |
| 510(k) | K132794 | SMARTVEST AIRWAY CLEARANCE SYSTEM | BYI | 2013-12-19 | View |
| 510(k) | K053248 | SMARTVEST AIRWAY CLEARANCE SYSTEM, MODEL TL | BYI | 2005-12-01 | View |
| 510(k) | K040367 | MEDPULSE RESPIRATORY VEST SYSTEM, MODEL 2000EZ | BYI | 2004-04-07 | View |
| 510(k) | K982889 | MEDPULSE RESPIRATORY VEST SYSTEM, MODEL 1000 | BYI | 1999-06-01 | View |
No matching devices.
Advertisement