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EUROLINE A312 SERIES OF BEHIND THE EAR AIR CONDUCTION HEARING AIDS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960494
510(k) Type
Traditional
Applicant
STARKEY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1996
Days to Decision
31 days
Submission Type
Summary