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Ameritek USA, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K071242DBEST ONE STEP OCCULT BLOOD TEST KITSMarch 6, 2008
K061257DBEST HCG PANEL TEST KITMay 4, 2007