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FULL DYNAMIC RANGE COMPRESSION BEHIND THE EAR HEARING INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951828
510(k) Type
Traditional
Applicant
SIEMENS HEARING INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1995
Days to Decision
71 days
Submission Type
Summary