Last synced on 2 December 2022 at 11:04 pm

RELIEVA ULTIRRA Sinus Balloon Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190525
510(k) Type
Traditional
Applicant
Acclarent, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2019
Days to Decision
60 days
Submission Type
Summary

RELIEVA ULTIRRA Sinus Balloon Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190525
510(k) Type
Traditional
Applicant
Acclarent, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2019
Days to Decision
60 days
Submission Type
Summary