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EVOK 900 SERIES HEARING AID/TINNITUS MASKER OPTION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093715
510(k) Type
Abbreviated
Applicant
MAGNATONE HEARING AID CORP. DBA PERSONA MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2010
Days to Decision
386 days
Submission Type
Summary

EVOK 900 SERIES HEARING AID/TINNITUS MASKER OPTION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093715
510(k) Type
Abbreviated
Applicant
MAGNATONE HEARING AID CORP. DBA PERSONA MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2010
Days to Decision
386 days
Submission Type
Summary