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EPIQ 5 Diagnostic Ultrasound System, EPIQ 7Diagnostic Ultrasound System, Affiniti 50 Diagnostic Ultrasound System, Affiniti 70 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160807
510(k) Type
Traditional
Applicant
PHILIPS ULTRASOUND, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2016
Days to Decision
13 days
Submission Type
Summary

EPIQ 5 Diagnostic Ultrasound System, EPIQ 7Diagnostic Ultrasound System, Affiniti 50 Diagnostic Ultrasound System, Affiniti 70 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160807
510(k) Type
Traditional
Applicant
PHILIPS ULTRASOUND, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2016
Days to Decision
13 days
Submission Type
Summary