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ACCLARENT AERA Eustachian Tube Balloon Dilation System

Page Type
Cleared 510(K)
510(k) Number
K171761
510(k) Type
Traditional
Applicant
Acclarent, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/2018
Days to Decision
216 days
Submission Type
Summary

ACCLARENT AERA Eustachian Tube Balloon Dilation System

Page Type
Cleared 510(K)
510(k) Number
K171761
510(k) Type
Traditional
Applicant
Acclarent, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/2018
Days to Decision
216 days
Submission Type
Summary