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EYEGLASS HEARING AID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K760609
510(k) Type
Traditional
Applicant
ZENITH HEARING INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/1976
Days to Decision
12 days