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Soundcure, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K150065
SoundCure Serenade Tinnitus Treatment System
April 13, 2015
K111293
SOUNDCURE SERENADE TINNITUS TREATMENT SYSTEM
August 24, 2011