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AXIOM SIRESKOP SD

Page Type
Cleared 510(K)
510(k) Number
K051602
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/2005
Days to Decision
21 days
Submission Type
Summary

AXIOM SIRESKOP SD

Page Type
Cleared 510(K)
510(k) Number
K051602
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/2005
Days to Decision
21 days
Submission Type
Summary