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Dymedso, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K103176
FREQUENCER
January 26, 2011
K100749
FREQUENCER MODEL V2X
August 31, 2010
K063645
FREQUENCER, MODEL 1001
March 15, 2007