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CORTISOL LIA

Page Type
Cleared 510(K)
510(k) Number
K010790
510(k) Type
Traditional
Applicant
KMI DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/2002
Days to Decision
320 days
Submission Type
Statement

CORTISOL LIA

Page Type
Cleared 510(K)
510(k) Number
K010790
510(k) Type
Traditional
Applicant
KMI DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/2002
Days to Decision
320 days
Submission Type
Statement