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Gn Resound A/S
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K150171
Tinnitus Sound Generator Module
May 14, 2015
K110932
TINNITUS SOUND GENERATOR MODULE
May 3, 2011
K073636
TINNITUS SOUND GENERATOR MODULE
March 13, 2008