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IN THE EAR HEARING AID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915450
510(k) Type
Traditional
Applicant
ZENITH/OMNI HEARING INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1992
Days to Decision
84 days
Submission Type
Statement