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MODULAR ANGIOGRAPHY SYSTEM AXIOM ARTIS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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