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CYCLASE ACTIVATING PTH (CAP) IMMUNORADIOMETRIC (IRMA) ASSAY KIT, MODEL 3KG001

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031534
510(k) Type
Traditional
Applicant
Scantibodies Laboratory, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2003
Days to Decision
75 days
Submission Type
Statement

CYCLASE ACTIVATING PTH (CAP) IMMUNORADIOMETRIC (IRMA) ASSAY KIT, MODEL 3KG001

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031534
510(k) Type
Traditional
Applicant
Scantibodies Laboratory, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2003
Days to Decision
75 days
Submission Type
Statement