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RESOUND CUSTOM IN-THE CANAL HEARING AID MODEL CA1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896463
510(k) Type
Traditional
Applicant
RESOUND CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1990
Days to Decision
87 days

RESOUND CUSTOM IN-THE CANAL HEARING AID MODEL CA1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896463
510(k) Type
Traditional
Applicant
RESOUND CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1990
Days to Decision
87 days