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RELIEVA AND RELIEVA ACELLA SINUS BALLOON CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073041
510(k) Type
Traditional
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/2008
Days to Decision
134 days
Submission Type
Summary

RELIEVA AND RELIEVA ACELLA SINUS BALLOON CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073041
510(k) Type
Traditional
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/2008
Days to Decision
134 days
Submission Type
Summary