Last synced on 14 November 2025 at 11:06 pm

IN-THE-EAR

Page Type
Cleared 510(K)
510(k) Number
K961827
510(k) Type
Traditional
Applicant
QUALITONE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/1996
Days to Decision
51 days
Submission Type
Summary

IN-THE-EAR

Page Type
Cleared 510(K)
510(k) Number
K961827
510(k) Type
Traditional
Applicant
QUALITONE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/1996
Days to Decision
51 days
Submission Type
Summary