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FDA 510(k) Applications Submitted by KENNETH R MICHAEL, PH.D.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K953233
07/10/1995
SIMVIEW 3000 CT OPTION
SIEMENS MEDICAL SOLUTIONS USA, INC.
K953391
07/19/1995
TREATMENT MANAGEMENT SYSTEM
SIEMENS MEDICAL SOLUTIONS USA, INC.
K130599
03/07/2013
WART FREEZE
KONINKLIJKE UTERMOHLEN NV
K962892
07/24/1996
HELAX TMS BRACHYTHERAPY, VERSION 3.0
SIEMENS MEDICAL SOLUTIONS USA, INC.
K954248
09/11/1995
SIEMENS VIRTURAL WEDGE
SIEMENS MEDICAL SOLUTIONS USA, INC.
K961902
05/16/1996
SIEMENS BEAM SHAPER
SIEMENS MEDICAL SOLUTIONS USA, INC.
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