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RELIEVA SINUS BALLOON CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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