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MULTIFLEX TINNITUS TECHNOLOGY

Page Type
Cleared 510(K)
510(k) Number
K122876
510(k) Type
Traditional
Applicant
STARKEY LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2012
Days to Decision
42 days
Submission Type
Summary

MULTIFLEX TINNITUS TECHNOLOGY

Page Type
Cleared 510(K)
510(k) Number
K122876
510(k) Type
Traditional
Applicant
STARKEY LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2012
Days to Decision
42 days
Submission Type
Summary