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MILENIA ESTRADIOL

Page Type
Cleared 510(K)
510(k) Number
K912917
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1991
Days to Decision
27 days
Submission Type
Statement

MILENIA ESTRADIOL

Page Type
Cleared 510(K)
510(k) Number
K912917
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1991
Days to Decision
27 days
Submission Type
Statement