510(K) Premarket Notification
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121 to 130 of 500 Results * |
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Device Name
|
Applicant
|
510(K)
Number |
Decision
Date |
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datex-ohmeda network and icentral '05, sales revision 4.3 | GE HEALTHCARE | k052972 |
12/29/2005 |
datex-ohmeda s/5 cardiac output and svo2 module, e-copsv and accessories | GE HEALTHCARE | k052977 |
11/22/2005 |
datex-ohmeda s/5 cardiac output module, e-cop and accessories | GE HEALTHCARE | k052976 |
01/13/2006 |
datex-ohmeda s/5 memory module, e-mem | GE HEALTHCARE | k052756 |
11/01/2005 |
datex-ohmeda s/5 nellcor compatible saturation module, e-nsat | GE HEALTHCARE | k052755 |
10/13/2005 |
datex-ohmeda s/5 web viewer, datex-ohmeda s/5 pocket viewer and datex-ohmeda s/5 cellular viewer with l-web04 software | GE HEALTHCARE | k052975 |
01/20/2006 |
dbest hcg panel test kit | AMERITEK USA, INC. | k061257 |
05/04/2007 |
del sol blue light therapy system | EDGE SYSTEMS CORPORATION | k061470 |
07/20/2006 |
deutsch anti-blockage wound drain | THE CATHETER EXCHANGE, INC. | k052286 |
10/21/2005 |
diacap ultra dialysis fluid filter | B. BRAUN MEDIZINTECHNOLOGIE GMBH | k052764 |
06/09/2006 |
* The maximum 500 records meeting your search criteria returned. Please narrow your search. |
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