Home / Companies / Karmelsonix

Karmelsonix

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K102229PULMOTRACK 2020 SYSTEMMarch 4, 2011
K101022PULMOTRACK 5050 WHOLTER, MODEL 5050July 9, 2010
K090863PERSONAL WHEEZOMETERSeptember 21, 2009
K071955WIM-PC, MODEL 1010November 1, 2007