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Karmelsonix

FDA Regulatory Profile

Karmelsonix appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 4, 2011.

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

FDA data resources