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PRIMOFOCUS COMPACT

Page Type
Cleared 510(K)
510(k) Number
K963788
510(k) Type
Traditional
Applicant
OTICON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1996
Days to Decision
68 days
Submission Type
Summary

PRIMOFOCUS COMPACT

Page Type
Cleared 510(K)
510(k) Number
K963788
510(k) Type
Traditional
Applicant
OTICON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1996
Days to Decision
68 days
Submission Type
Summary