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MODULAR ANGIOGRAPHY SYSTEM AXIOM ARTIS

Page Type
Cleared 510(K)
510(k) Number
K021021
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/2002
Days to Decision
69 days
Submission Type
Summary

MODULAR ANGIOGRAPHY SYSTEM AXIOM ARTIS

Page Type
Cleared 510(K)
510(k) Number
K021021
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/2002
Days to Decision
69 days
Submission Type
Summary