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Acclarent Aera Eustachian Tube Balloon Dilation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN150056
510(k) Type
Direct
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Deleted
Decision Date
9/16/2016
Days to Decision
284 days

Acclarent Aera Eustachian Tube Balloon Dilation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN150056
510(k) Type
Direct
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Deleted
Decision Date
9/16/2016
Days to Decision
284 days