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Activatek, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K132832ACTIVAPATCH ET IONTOPHORESIS PATCHFebruary 13, 2014
K091326ACTIVAPATCHMay 27, 2009
K061522TRIVARION BUFFERED IONTOPHORESIS ELECTRODE SYSTEMAugust 1, 2006