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Armadillo Biomedical, 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
K142914
DacryoCATH
January 12, 2015
K113508
DACRYOCATH
August 31, 2012