FDA 510(k) Applications Submitted by SANDRA ROBINSON

FDA 510(k) Number Submission Date Device Name Applicant
K021021 03/29/2002 MODULAR ANGIOGRAPHY SYSTEM AXIOM ARTIS SIEMENS MEDICAL SOLUTIONS USA, INC.
K013826 11/19/2001 AXIOM ARISTOS FX (MULTI PURPOSE RADIOGRAPHY SYSTEM) SIEMENS MEDICAL SYSTEMS, INC.
K014113 12/14/2001 ENDOMAP SIEMENS MEDICAL SOLUTIONS USA, INC.


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