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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