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RELIEVA SEEKER BALLOON SINUPLASTY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K120280
510(k) Type
Traditional
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2012
Days to Decision
280 days
Submission Type
Summary

RELIEVA SEEKER BALLOON SINUPLASTY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K120280
510(k) Type
Traditional
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2012
Days to Decision
280 days
Submission Type
Summary