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HUMAN CHORIONIC GONADOTROPIN VISUAL TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K880410
510(k) Type
Traditional
Applicant
DISEASE DETECTION INTERNATIONAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/1988
Days to Decision
64 days

HUMAN CHORIONIC GONADOTROPIN VISUAL TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K880410
510(k) Type
Traditional
Applicant
DISEASE DETECTION INTERNATIONAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/1988
Days to Decision
64 days