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NEO-PREGNOSTICON DUOCLON TUBE TEST

Page Type
Cleared 510(K)
510(k) Number
K831339
510(k) Type
Traditional
Applicant
ORGANON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/1983
Days to Decision
44 days

NEO-PREGNOSTICON DUOCLON TUBE TEST

Page Type
Cleared 510(K)
510(k) Number
K831339
510(k) Type
Traditional
Applicant
ORGANON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/1983
Days to Decision
44 days