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SEQUOIA PLUS DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K072365
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2007
Days to Decision
55 days
Submission Type
Summary

SEQUOIA PLUS DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K072365
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2007
Days to Decision
55 days
Submission Type
Summary