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Ikoetech, LLC
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K083591
IKOENGELO, VERSION 2
December 29, 2008
K061006
IKOENGELO
June 5, 2006