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OTICON /PRIMOFOCUS (PF)

Page Type
Cleared 510(K)
510(k) Number
K960284
510(k) Type
Traditional
Applicant
OTICON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1996
Days to Decision
48 days
Submission Type
Statement

OTICON /PRIMOFOCUS (PF)

Page Type
Cleared 510(K)
510(k) Number
K960284
510(k) Type
Traditional
Applicant
OTICON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1996
Days to Decision
48 days
Submission Type
Statement