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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