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RELIEVA SCOUT SINUS DILATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K140160
510(k) Type
Special
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/2014
Days to Decision
29 days
Submission Type
Summary

RELIEVA SCOUT SINUS DILATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K140160
510(k) Type
Special
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/2014
Days to Decision
29 days
Submission Type
Summary