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Sentio Ti Implant Kit; Sentio 1 Mini; Genie Medical BAHS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240614
510(k) Type
Traditional
Applicant
Oticon Medical AB
Country
Sweden
FDA Decision
Substantially Equivalent
Decision Date
7/10/2024
Days to Decision
127 days
Submission Type
Summary

Sentio Ti Implant Kit; Sentio 1 Mini; Genie Medical BAHS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240614
510(k) Type
Traditional
Applicant
Oticon Medical AB
Country
Sweden
FDA Decision
Substantially Equivalent
Decision Date
7/10/2024
Days to Decision
127 days
Submission Type
Summary