Last synced on 14 November 2025 at 11:06 pm

RELIEVA SPIN SINUS DILATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K111875
510(k) Type
Traditional
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2011
Days to Decision
102 days
Submission Type
Summary

RELIEVA SPIN SINUS DILATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K111875
510(k) Type
Traditional
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2011
Days to Decision
102 days
Submission Type
Summary