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RETROX TITANIUM TUBE SYSTEM FOR THE RETROX TRANSCUTANEOUS AIR CONDUCTION HEARING AID SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040996
510(k) Type
Traditional
Applicant
GYRUS ENT L.L.C.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/2004
Days to Decision
126 days
Submission Type
Summary

RETROX TITANIUM TUBE SYSTEM FOR THE RETROX TRANSCUTANEOUS AIR CONDUCTION HEARING AID SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040996
510(k) Type
Traditional
Applicant
GYRUS ENT L.L.C.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/2004
Days to Decision
126 days
Submission Type
Summary