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DUOCLON SLIDE TEST

Page Type
Cleared 510(K)
510(k) Number
K831109
510(k) Type
Traditional
Applicant
ORGANON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/1983
Days to Decision
58 days

DUOCLON SLIDE TEST

Page Type
Cleared 510(K)
510(k) Number
K831109
510(k) Type
Traditional
Applicant
ORGANON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/1983
Days to Decision
58 days