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RELIEVA SOLO ELITE SINUS BALLOON CATHETER

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