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PREGNOSTICON PREGNANCY TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K790734
510(k) Type
Traditional
Applicant
ORGANON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/1979
Days to Decision
60 days

PREGNOSTICON PREGNANCY TEST KIT

Page Type
Cleared 510(K)
510(k) Number
K790734
510(k) Type
Traditional
Applicant
ORGANON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/1979
Days to Decision
60 days