Electromed, Inc.
Electromed, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 6 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 18, 2022.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 6
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K222496 | Electromed SmartVest Airway Clearance System | November 18, 2022 |
| K132794 | SMARTVEST AIRWAY CLEARANCE SYSTEM | December 19, 2013 |
| K053248 | SMARTVEST AIRWAY CLEARANCE SYSTEM, MODEL TL | December 1, 2005 |
| K040367 | MEDPULSE RESPIRATORY VEST SYSTEM, MODEL 2000EZ | April 7, 2004 |
| K982889 | MEDPULSE RESPIRATORY VEST SYSTEM, MODEL 1000 | June 1, 1999 |
| K990813 | REHCOR | April 12, 1999 |