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Gn Resound A/S

FDA Regulatory Profile

Gn Resound A/S appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 14, 2015.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K150171Tinnitus Sound Generator ModuleMay 14, 2015
K110932TINNITUS SOUND GENERATOR MODULEMay 3, 2011
K073636TINNITUS SOUND GENERATOR MODULEMarch 13, 2008

FDA data resources