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ANGIOSTAR

Page Type
Cleared 510(K)
510(k) Number
K884912
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/16/1989
Days to Decision
80 days

ANGIOSTAR

Page Type
Cleared 510(K)
510(k) Number
K884912
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/16/1989
Days to Decision
80 days