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CORTISOL LIA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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