FDA 510(k) Applications Submitted by VISTA MEDICAL TECHNOLOGIES, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K961800 |
05/09/1996 |
HEAD MOUNTED DISPLAY |
VISTA MEDICAL TECHNOLOGIES, INC. |
K020301 |
01/29/2002 |
MODIFICATION TO VISTA STEREOSCOPE SYSTEM |
VISTA MEDICAL TECHNOLOGIES, INC. |
K021290 |
04/23/2002 |
VISTA VISUALIZATION SYSTEM, MODEL 9000, VISTA VISUALIZATION SYSTEM WITH VOICE ACTIVATION AND PIP, MODEL 9100 |
VISTA MEDICAL TECHNOLOGIES, INC. |
K970217 |
01/21/1997 |
VISTA ILLUMINATION SYSTEM |
VISTA MEDICAL TECHNOLOGIES, INC. |
K971373 |
04/14/1997 |
VISTA SINGLE CHIP VIDEO CAMERA |
VISTA MEDICAL TECHNOLOGIES, INC. |
K973436 |
09/10/1997 |
VISTA HEAD MOUNTED DISPLAY |
VISTA MEDICAL TECHNOLOGIES, INC. |
K991303 |
04/16/1999 |
VISTA ORPC WITH INFOMATIX INTRAOP SOFTWARE |
VISTA MEDICAL TECHNOLOGIES, INC. |
K990635 |
02/26/1999 |
VISTA STEREOSCOPE SYSTEM |
VISTA MEDICAL TECHNOLOGIES, INC. |
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