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MILENIA PROGESTERONE

Page Type
Cleared 510(K)
510(k) Number
K911512
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/1991
Days to Decision
48 days

MILENIA PROGESTERONE

Page Type
Cleared 510(K)
510(k) Number
K911512
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/1991
Days to Decision
48 days