Electromed, Inc.
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest FDA decision2022-11-18
SEC Filings: 1 filings on record. Latest: 8-K (2026-08-25). View on SEC EDGAR →
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K222496 | Electromed SmartVest Airway Clearance System | BYI | 2022-11-18 | View |
No matching devices.