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Activatek, Inc.

FDA Regulatory Profile

Activatek, Inc. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 13, 2014.

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

FDA data resources