Last synced on 14 November 2025 at 11:06 pm

STARKEY TM-3, TM-5 HIGH FREQUENCY TINNITUS MASKER

Page Type
Cleared 510(K)
510(k) Number
K964216
510(k) Type
Traditional
Applicant
STARKEY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/1996
Days to Decision
45 days
Submission Type
Summary

STARKEY TM-3, TM-5 HIGH FREQUENCY TINNITUS MASKER

Page Type
Cleared 510(K)
510(k) Number
K964216
510(k) Type
Traditional
Applicant
STARKEY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/1996
Days to Decision
45 days
Submission Type
Summary