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RELIEVA SINUS BALLOON INFLATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K052198
510(k) Type
Traditional
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/2005
Days to Decision
19 days
Submission Type
Summary

RELIEVA SINUS BALLOON INFLATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K052198
510(k) Type
Traditional
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/2005
Days to Decision
19 days
Submission Type
Summary