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ANGIO-CT MIYABI

Page Type
Cleared 510(K)
510(k) Number
K990491
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/1999
Days to Decision
47 days
Submission Type
Summary

ANGIO-CT MIYABI

Page Type
Cleared 510(K)
510(k) Number
K990491
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/1999
Days to Decision
47 days
Submission Type
Summary