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DIGDOP ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K090465
510(k) Type
Traditional
Applicant
THE NEWMAN GROUP, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/2009
Days to Decision
44 days
Submission Type
Statement

DIGDOP ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K090465
510(k) Type
Traditional
Applicant
THE NEWMAN GROUP, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/2009
Days to Decision
44 days
Submission Type
Statement