FDA 510(k) Applications Submitted by VIVANT MEDICAL, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K003439 |
11/06/2000 |
VIVANT BREAST LESION LOCALIZATION DEVICE |
VIVANT MEDICAL, INC. |
K000278 |
01/31/2000 |
VIVANT MEDICAL BIOPSY MARKER SYSTEM |
VIVANT MEDICAL, INC. |
K050223 |
01/31/2005 |
VIVAWAVE MICROWAVE ABLATION SYSTEM, COAXIAL INTRODUCER |
VIVANT MEDICAL, INC. |
K040279 |
02/05/2004 |
VIVARING MICROWAVE ABLATION PROBE |
VIVANT MEDICAL, INC. |
K031556 |
05/19/2003 |
VIVATHERM THEMPERATURE MEASUREMENT SYSTEM |
VIVANT MEDICAL, INC. |
K011676 |
05/30/2001 |
VIVAWAVE MICROWAVE SYSTEM |
VIVANT MEDICAL, INC. |
K032047 |
07/02/2003 |
TRI-LOOP MICROWAVE ABLATION PROBE |
VIVANT MEDICAL, INC. |
K022286 |
07/15/2002 |
ENCIRCLE LOCALIZATION DEVICE |
VIVANT MEDICAL, INC. |
K032702 |
09/02/2003 |
VIVATIP MICROWAVE ABLATION PROBE |
VIVANT MEDICAL, INC. |
K023311 |
10/03/2002 |
LOOP MICROWAVE ABLATION PROBE |
VIVANT MEDICAL, INC. |
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