FDA 510(k) Applications Submitted by INFINITT CO., LTD.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K041500 |
06/07/2004 |
STARPACS ORTHOPEDICS SYSTEM |
INFINITT CO., LTD. |
K111613 |
06/09/2011 |
XELIS FUSION |
INFINITT CO., LTD. |
K111660 |
06/14/2011 |
XELIS CARDIAC |
INFINITT CO., LTD. |
K051715 |
06/27/2005 |
STARPACS DENTAL |
INFINITT CO., LTD. |
K041761 |
06/30/2004 |
RAPIDIACOLON |
INFINITT CO., LTD. |
K052284 |
08/22/2005 |
REFORMAT GATEWAY |
INFINITT CO., LTD. |
K052545 |
09/15/2005 |
INFINITT G3 PACS |
INFINITT CO., LTD. |
K082706 |
09/16/2008 |
INFINITT CARDIOLOGY PACS |
INFINITT CO., LTD. |
K103130 |
10/22/2010 |
XELIS 3D |
INFINITT CO., LTD. |
K163290 |
11/22/2016 |
INFINITT ULite |
INFINITT CO., LTD. |
K102684 |
09/17/2010 |
XELIS DENTAL |
INFINITT CO., LTD. |
K082990 |
10/07/2008 |
INFINITT XELIS |
INFINITT CO., LTD. |
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