Last synced on 14 November 2025 at 11:06 pm

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

Page Type
Cleared 510(K)
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)
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