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Epitek, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K080780ANCHORAGE SCOPE, MODEL 000003July 30, 2008
K073507ANCHORAGE ACCESS KITMarch 5, 2008
K073096ANCHORAGE CLOSURE DEVICEFebruary 7, 2008