Last synced on 30 May 2025 at 11:05 pm

TOTAL PTH IMMUNORADIOMETRIC ASSAY(IRMA) DIAGNOSTIC KIT, MODEL 3KG600

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K004038
510(k) Type
Traditional
Applicant
SCANTIBODIES LABORATORY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/2001
Days to Decision
123 days
Submission Type
Statement

TOTAL PTH IMMUNORADIOMETRIC ASSAY(IRMA) DIAGNOSTIC KIT, MODEL 3KG600

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K004038
510(k) Type
Traditional
Applicant
SCANTIBODIES LABORATORY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/2001
Days to Decision
123 days
Submission Type
Statement