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FDA 510(k) Applications Submitted by Martin Newman
FDA 510(k) Number
Submission Date
Device Name
Applicant
K970214
01/21/1997
3 DIMENSIONAL VIDEO ENDOSCOPE
OKTAS
K970217
01/21/1997
VISTA ILLUMINATION SYSTEM
VISTA MEDICAL TECHNOLOGIES, INC.
K970369
01/31/1997
VISTA MINI CAMERA SYSTEM
OKTAS
K200849
03/31/2020
Tempus LS - Manual
Remote Diagnostic Technologies, Ltd, a Philips Company
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.
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