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DIGIFOCUS COMPACT

Page Type
Cleared 510(K)
510(k) Number
K961059
510(k) Type
Traditional
Applicant
OTICON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/1996
Days to Decision
50 days
Submission Type
Summary

DIGIFOCUS COMPACT

Page Type
Cleared 510(K)
510(k) Number
K961059
510(k) Type
Traditional
Applicant
OTICON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/1996
Days to Decision
50 days
Submission Type
Summary