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AXIOM ARISTOS FX (MULTI PURPOSE RADIOGRAPHY SYSTEM)

Page Type
Cleared 510(K)
510(k) Number
K013826
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2002
Days to Decision
74 days
Submission Type
Summary

AXIOM ARISTOS FX (MULTI PURPOSE RADIOGRAPHY SYSTEM)

Page Type
Cleared 510(K)
510(k) Number
K013826
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2002
Days to Decision
74 days
Submission Type
Summary