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Remicalm, LLC
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K090135
TRIMIRA IDENTAFI 3000
February 17, 2009
K082603
TRIMIRA OCS 3000
December 12, 2008