Last synced on 2 May 2025 at 11:05 pm

TULA Iontophoresis System with Earset

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150453
510(k) Type
Special
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/2015
Days to Decision
89 days
Submission Type
Summary

TULA Iontophoresis System with Earset

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150453
510(k) Type
Special
Applicant
ACCLARENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/2015
Days to Decision
89 days
Submission Type
Summary