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ACTH IMMUNORADIOMETRIC (IRMA) DIAGNOSTIC ASSAY KIT, MODEL #3KG100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021032
510(k) Type
Traditional
Applicant
SCANTIBODIES LABORATORY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2002
Days to Decision
66 days
Submission Type
Statement

ACTH IMMUNORADIOMETRIC (IRMA) DIAGNOSTIC ASSAY KIT, MODEL #3KG100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021032
510(k) Type
Traditional
Applicant
SCANTIBODIES LABORATORY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2002
Days to Decision
66 days
Submission Type
Statement