Company ยท US
Electromed, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2022. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Nov 18, 2022 | K222496 | Electromed SmartVest Airway Clearance System Electromed, Inc. | BYI |
| Dec 19, 2013 | K132794 | SMARTVEST AIRWAY CLEARANCE SYSTEM Electromed, Inc. | BYI |
| Dec 1, 2005 | K053248 | SMARTVEST AIRWAY CLEARANCE SYSTEM, MODEL TL Electromed, Inc. | BYI |
| Apr 7, 2004 | K040367 | MEDPULSE RESPIRATORY VEST SYSTEM, MODEL 2000EZ Electromed, Inc. | BYI |
| Jun 1, 1999 | K982889 | MEDPULSE RESPIRATORY VEST SYSTEM, MODEL 1000 Electromed, Inc. | BYI |
| Apr 12, 1999 | K990813 | REHCOR Electromed Corp. | ISD |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||