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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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