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NUVIS DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K133833
510(k) Type
Traditional
Applicant
PHILIPS ULTRASOUND, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2014
Days to Decision
31 days
Submission Type
Summary

NUVIS DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K133833
510(k) Type
Traditional
Applicant
PHILIPS ULTRASOUND, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2014
Days to Decision
31 days
Submission Type
Summary