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Sensormed
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K113330
CABLECAP
January 12, 2012
K101496
CABLECAP MODEL: WLF, STZ, ACM
September 14, 2010