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HEARING AID (ALL-IN-THE-EAR)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K873490
510(k) Type
Traditional
Applicant
KERR HEARING AID LABORATORY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1987
Days to Decision
73 days