Last synced on 25 April 2025 at 11:05 pm

EPIQ 5 Diagnostic Ultrasound System; EPIQ 7 Diagnostic 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
K163120
510(k) Type
Traditional
Applicant
Philips Ultrasound, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2017
Days to Decision
63 days
Submission Type
Summary

EPIQ 5 Diagnostic Ultrasound System; EPIQ 7 Diagnostic 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
K163120
510(k) Type
Traditional
Applicant
Philips Ultrasound, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2017
Days to Decision
63 days
Submission Type
Summary