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Electromed Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
5
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K222496Electromed SmartVest Airway Clearance SystemNovember 18, 2022
K132794SMARTVEST AIRWAY CLEARANCE SYSTEMDecember 19, 2013
K053248SMARTVEST AIRWAY CLEARANCE SYSTEM, MODEL TLDecember 1, 2005
K040367MEDPULSE RESPIRATORY VEST SYSTEM, MODEL 2000EZApril 7, 2004
K982889MEDPULSE RESPIRATORY VEST SYSTEM, MODEL 1000June 1, 1999
K990813REHCORApril 12, 1999