FDA 510(k) Applications Submitted by XOFT, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K072616 |
09/17/2007 |
AXXENT VAGINAL APPLICATOR |
XOFT, INC. |
K072683 |
09/21/2007 |
AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM |
XOFT, INC. |
K050843 |
04/01/2005 |
AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM |
XOFT, INC. |
K090417 |
02/18/2009 |
AXXENT FLEXISHIELD MINI |
XOFT, INC. |
K090914 |
04/01/2009 |
AXXENT BALLOON APPLICATOR, MODEL AB2034, AB2045, AB2056, AB2057E, AB2067E |
XOFT, INC. |
K083734 |
12/16/2008 |
AXXENT SURFACE APPLICATOR, MODEL 710257 |
XOFT, INC. |
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