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TELEX IN-THE-EAR CUSTOM HEARING AID WITH THRESHOLD COMPRESSION-II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964639
510(k) Type
Traditional
Applicant
TELEX COMMUNICATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/1997
Days to Decision
63 days
Submission Type
Summary