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RELIEVA SOLO ELITE SINUS BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K111254
510(k) Type
Traditional
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2011
Days to Decision
110 days
Submission Type
Summary

RELIEVA SOLO ELITE SINUS BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K111254
510(k) Type
Traditional
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2011
Days to Decision
110 days
Submission Type
Summary