Last synced on 10 January 2025 at 11:05 pm

ACCLARENT SE Inflation Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150172
510(k) Type
Special
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2015
Days to Decision
71 days
Submission Type
Summary

ACCLARENT SE Inflation Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150172
510(k) Type
Special
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2015
Days to Decision
71 days
Submission Type
Summary