Last synced on 10 January 2025 at 11:05 pm

Multiflex Tinnitus Technology

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201370
510(k) Type
Special
Applicant
Starkey Laboratories, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/2020
Days to Decision
28 days
Submission Type
Summary

Multiflex Tinnitus Technology

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201370
510(k) Type
Special
Applicant
Starkey Laboratories, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/2020
Days to Decision
28 days
Submission Type
Summary