FDA 510(k) Applications Submitted by CAROL A DEPOUW
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K130321 |
02/08/2013 |
LIAISON ALDOSTERONE, LIAISON ALDOSTERONE CONTROL SET, LIAISON ALDOSTERONE CALIBRATION VERIFIERS |
DIASORIN |
| K061247 |
05/03/2006 |
DIASORIN LIAISON TREPONEMA ASSAY |
DIASORIN, INC. |
| K141463 |
06/03/2014 |
LIASON XL1,25 DIHYDROXYVITAMIN D; CONTROL SET, CALIBRATION VERIFIERS |
DiaSorin Inc. |
| K081685 |
06/17/2008 |
LIAISON HSV-1 TYPE SPECIFIC IGG ASSAY, CONTROL HSV-1 IGG |
DIASORIN, INC. |
| K081687 |
06/17/2008 |
LIAISON HSV-2 TYPE SPECIFIC IGG ASSAY, CONTROL HSV-2 IGG |
DIASORIN, INC. |
| K082049 |
07/18/2008 |
LIAISON ANTI-HAV ASSAY, LIAISON CONTROL ANTI-HAV |
DIASORIN, INC. |
| K082050 |
07/18/2008 |
LIAISON HAV IGM ASSAY, LIAISON CONTROL HAV IGM |
DIASORIN, INC. |
| K122397 |
08/07/2012 |
LIAISON RUBELLA IGM, LIAISON CONTROL RUBELLA IGM |
DIASORIN, INC. |
| K132515 |
08/12/2013 |
LIAISON N-TACT PTH GEN II, CONTROL SET, CALIBRATION VERIFIERS |
DIASORIN, INC. |
| K062473 |
08/24/2006 |
LIAISON BORRELIA IGG/IGM ASSAY, MODEL 310870; SERUM CONTROLS, MODEL 310871 |
DIASORIN, INC. |
| K052794 |
10/03/2005 |
ETI-MAX 3000 |
DIASORIN, INC. |
| K093498 |
11/12/2009 |
LIAISON N-TACT PTH CALIBRATION VERIFIERS MODEL 310913 |
DIASORIN, INC. |
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