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DELFIA(R) 17 -OH-PROGESTERON KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912026
510(k) Type
Traditional
Applicant
PHARMACIA DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/1991
Days to Decision
49 days
Submission Type
Statement

DELFIA(R) 17 -OH-PROGESTERON KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912026
510(k) Type
Traditional
Applicant
PHARMACIA DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/1991
Days to Decision
49 days
Submission Type
Statement