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Multiflex Tinnitus Technology

Page Type
Cleared 510(K)
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)
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