Last synced on 19 July 2024 at 11:05 pm

IN-THE-EAR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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