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TINNITUS THERAPY SYSTEM ANM T30 CR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112752
510(k) Type
Traditional
Applicant
ANM ADAPTIVE NEUROMODULATION GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
12/16/2011
Days to Decision
86 days
Submission Type
Summary

TINNITUS THERAPY SYSTEM ANM T30 CR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112752
510(k) Type
Traditional
Applicant
ANM ADAPTIVE NEUROMODULATION GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
12/16/2011
Days to Decision
86 days
Submission Type
Summary