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WHOLE PTH (1-84) SPECIFIC IMMUNORADIOMETRIC IRMA DIAGNOSTIC ASSAY KIT, MODEL 3KG056

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001411
510(k) Type
Traditional
Applicant
Scantibodies Laboratory, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2000
Days to Decision
109 days
Submission Type
Statement

WHOLE PTH (1-84) SPECIFIC IMMUNORADIOMETRIC IRMA DIAGNOSTIC ASSAY KIT, MODEL 3KG056

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001411
510(k) Type
Traditional
Applicant
Scantibodies Laboratory, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2000
Days to Decision
109 days
Submission Type
Statement