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RELIEVA SINUS BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K061903
510(k) Type
Special
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/2006
Days to Decision
44 days
Submission Type
Summary

RELIEVA SINUS BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K061903
510(k) Type
Special
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/2006
Days to Decision
44 days
Submission Type
Summary