FDA 510(k) Applications Submitted by MICHAEL NORDSTROM

FDA 510(k) Number Submission Date Device Name Applicant
K060348 02/10/2006 MODIFICATION TO: TOTAL INTACT PTH IMMUNOCHEMILUMINOMETRIC (ICMA) ASSAY KIT SCANTIBODIES LABORATORY, INC.
K060420 02/17/2006 MODIFICATION TO WHOLE PTH (1-84) SPECIFIC IMMUNOCHEMILLUMINOMETRIC (ICMA) ASSAY KIT, MODEL 3KG002 SCANTIBODIES LABORATORY, INC.
K060578 03/06/2006 CALCITONIN IMMUNORADIOMETRIC ASSAY (IRMA) (COATED TUBE VERSION) SCANTIBODIES LABORATORY, INC.
K050748 03/22/2005 ACTH IMMUNORADIOMETRIC (IRMA) ASSAY KIT, MODEL 3KG011 SCANTIBODIES LABORATORY, INC.
K051141 05/04/2005 WHOLE PTH (1-84) SPECIFIC IMMUNOCHEMILUMINOMETRIC ASSAY (ICMA), MODEL 3KG002 SCANTIBODIES LABORATORY, INC.
K051150 05/04/2005 TOTAL INTACT PTH IMMUNOCHEMILUMINOMETRIC (ICMA) ASSAY KIT SCANTIBODIES LABORATORY, INC.
K051810 07/05/2005 WHOLE PTH (1-84) SPECIFIC IMMUNORADIOMETRIC ASSAY (IRMA) COATED TUBE KIT, MODEL 3KG014 SCANTIBODIES LABORATORY, INC.
K051888 07/12/2005 TOTAL INTACT PTH IMMUNORADIOMETRIC ASSAY (COATED TUBE VERSION), MODEL 3KG013 SCANTIBODIES LABORATORY, INC.


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