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SONOLINE CF

Page Type
Cleared 510(K)
510(k) Number
K891449
510(k) Type
Traditional
Applicant
SIEMENS ULTRASOUND, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/1989
Days to Decision
204 days

SONOLINE CF

Page Type
Cleared 510(K)
510(k) Number
K891449
510(k) Type
Traditional
Applicant
SIEMENS ULTRASOUND, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/1989
Days to Decision
204 days