Last synced on 27 January 2023 at 11:04 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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